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: 0.13 (A)
Location

Chromosome 1:12164182 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1201257, rs61532883

HGVS name

1:g.12164182C>A

This variation has assays on 11 chips - click the plus to show

Variation displays