Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.27 (T)
Location

Chromosome 17:15368756 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60985500, rs117224224

HGVS name

17:g.15368756G>T

This variation has assays on 10 chips - click the plus to show

Variation displays