Original source

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

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

Chromosome 9:27556055 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs61629529

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 5 sample genotypes.

Variant displays