Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.13 (C)
Location

Chromosome 11:72056550 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3018309, rs61408328

This variation has 18 HGVS names - click the plus to show

Variation displays