Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.31 (G)
Location

Chromosome 11:65955144 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1190942, rs1151535, rs1191203

This variation has 5 HGVS names - click the plus to show

Variation displays