Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: HMGB2 (Hsa)
(GRCh38)4:173332154C>T
(Homo sapiens)Allele/Variant
Source: rs972446846
Genes: HMGB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:173332154C>T
(GRCh38)4:173332143A>C
(Homo sapiens)Allele/Variant
Source: rs776576177
Genes: HMGB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:173332143A>C
(GRCh38)4:173333197C>A
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.173333197C>A
Genes: HMGB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:173333197C>A
(GRCh38)4:173332217T>C
(Homo sapiens)Allele/Variant
Source: rs137965801
Genes: HMGB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:173332217T>C
(GRCh38)4:173332109C>T
(Homo sapiens)Allele/Variant
Source: rs1297919338
Genes: HMGB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:173332109C>T