Original source

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

G/A|Ancestral: A|Ambiguity code: R|MAF: 0.43 (A)

Chromosome 15:67154447 (forward strand)|View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs60845077, rs17293687

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on 15 chips - Show

About this variant

This variant overlaps 9 transcripts, has 4310 sample genotypes, is associated with 1 phenotype and is mentioned in 7 citations.

Variant displays