Original source

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

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

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