Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.22 (C)
Location

Chromosome 11:34940209 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60593547

This variation has 6 HGVS names - click the plus to show

Variation displays