Original source

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

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

Chromosome 9:114806486 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR091269

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59159913

HGVS name

9:g.114806486A>G

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

Variation displays