Original source

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

T/A | Ancestral: T | Ambiguity code: W

Chromosome 19:10133368 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs3209915

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 1 sample genotype.

Variant displays