Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60163996, rs17577917

This variation has 3 HGVS names - click the plus to show

This variation has assays on 12 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 4297 individual genotypes.

Variation displays