Original source

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

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

Chromosome 1:192536813 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60598391, rs12734298

HGVS name

1:g.192536813C>A

This variation has assays on 10 chips - click the plus to show

Variation displays