Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 17:47252316 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60342595, rs3809859

HGVS name

17:g.47252316G>A

This variation has assays on 9 chips - click the plus to show

Variation displays