Original source

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

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

Chromosome 3:185512895 (forward strand) | View in location tab

Most severe consequence
Intron variant
HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 173 sample genotypes.

Variant displays