Version: 8.0.0
Date: Tue Jan 28 2025
3 results
Allele/Variant Genes: SNCG (Hsa) Molecular Consequence: 3 prime UTR variant

(GRCh38)10:86962974G>A

(Homo sapiens)
Allele/Variant
Source: rs374301169
Genes: MMRN2 (Hsa), SNCG (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:86962974G>A

(GRCh38)10:86962974G>T

(Homo sapiens)
Allele/Variant
Source: rs374301169
Genes: MMRN2 (Hsa), SNCG (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:86962974G>T

(GRCh38)10:86962661G>C

(Homo sapiens)
Allele/Variant
Source: rs779800178
Genes: MMRN2 (Hsa), SNCG (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:86962661G>C