Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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