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: 0.10 (A)
Location

Chromosome 11:116837538 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR961720

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61758320, rs17249491

This variation has 7 HGVS names - click the plus to show

Variation displays