Version: 8.0.0
Date: Tue Jan 28 2025
15 results
Allele/Variant Genes: DKK2 (Hsa)

(GRCh38)4:106924560T>A

(Homo sapiens)
Allele/Variant
Source: rs374743911
Genes: DKK2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:106924560T>A

(GRCh38)4:106925949C>T

(Homo sapiens)
Allele/Variant
Source: rs201073614
Genes: DKK2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:106925949C>T

(GRCh38)4:107035572C>T

(Homo sapiens)
Allele/Variant
Source: rs147012957
Genes: DKK2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:107035572C>T

(GRCh38)4:106923995A>T

(Homo sapiens)
Allele/Variant
Source: rs1282726784
Genes: DKK2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:106923995A>T

(GRCh38)4:106924082G>A

(Homo sapiens)
Allele/Variant
Source: rs753265155
Genes: DKK2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:106924082G>A

(GRCh38)4:107046609A>G

(Homo sapiens)
Allele/Variant
Source: rs207464938
Genes: DKK2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:107046609A>G

(GRCh38)4:106924168C>G

(Homo sapiens)
Allele/Variant
Source: rs772632334
Genes: DKK2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:106924168C>G

(GRCh38)4:106925861C>T

(Homo sapiens)
Allele/Variant
Source: rs541386879
Genes: DKK2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:106925861C>T

(GRCh38)4:106925880A>G

(Homo sapiens)
Allele/Variant
Source: rs769686573
Genes: DKK2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:106925880A>G

(GRCh38)4:106924601T>C

(Homo sapiens)
Allele/Variant
Source: rs1348128917
Genes: DKK2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:106924601T>C

(GRCh38)4:106924040C>T

(Homo sapiens)
Allele/Variant
Source: rs768079972
Genes: DKK2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:106924040C>T

(GRCh38)4:106925879G>A

(Homo sapiens)
Allele/Variant
Source: rs267599976
Genes: DKK2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:106925879G>A

(GRCh38)4:106925871T>C

(Homo sapiens)
Allele/Variant
Source: rs202160269
Genes: DKK2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, start_lost
Diseases: Not Available
Variant Name: (GRCh38)4:106925871T>C

(GRCh38)4:107194929A>T

(Homo sapiens)
Allele/Variant
Source: rs207464939
Genes: DKK2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:107194929A>T

(GRCh38)4:107035585C>T

(Homo sapiens)
Allele/Variant
Source: rs772738812
Genes: DKK2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:107035585C>T