Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.38 (A)

Chromosome 1:169476945 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs60163996, rs17577917

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 3 transcripts, has 4297 sample genotypes and is associated with 1 phenotype.

Variant displays