Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

T/C | Ancestral: T | Ambiguity code: Y | MAF: < 0.01 (C)

Chromosome 1:155289124 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs185632402

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 6 transcripts, has 2504 sample genotypes and is mentioned in 1 citation.

Variant displays