Original source

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

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

Chromosome 1:115294971 (forward strand) | View in location tab

Most severe consequence
Intron variant
HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 267 sample genotypes.

Variant displays