Original source

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

G/A/C | Ancestral: G | Ambiguity code: V | MAF: 0.02 (A)

Chromosome 7:7369747 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs117476619, rs17515238

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2578 sample genotypes.

Variant displays