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 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