Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.02 (A)
Location

Chromosome 14:22970256 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60367674, rs58880345

HGVS name

14:g.22970256A>C

This variation has assays on 4 chips - click the plus to show

Variation displays