Original source

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

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

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60845077, rs17293687

This variation has 10 HGVS names - click the plus to show

This variation has assays on 15 chips - click the plus to show

About this variant

This variant overlaps 9 transcripts, has 4310 individual genotypes, is associated with 1 phenotype and is mentioned in 5 citations.

Variation displays