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: 0.47 (A)
Location

Chromosome 11:119184653 (forward strand) | View in location tab

Co-located

with dbSNP rs78643667 (A/G)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58180459

HGVS name

11:g.119184653A>G

Variation displays