Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.30 (A)
Location

Chromosome 17:45329682 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60342595, rs3809859

HGVS name

17:g.45329682G>A

This variation has assays on 7 chips - click the plus to show

Variation displays