Original source

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

Alleles
G/A/T|Ancestral: G|Ambiguity code: D|MAF: < 0.01 (A)
Location

Chromosome 15:74043070 (forward strand)|View in location tab

Most severe consequence
 
Stop gained
Evidence status

HGVS names

This variant has 24 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and has 2766 sample genotypes.

Variant displays