This variation maps to 8 locations

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Original source

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

C/A | Ancestral: C | Ambiguity code: M | MAF: 0.04 (A)

This variation maps to 8 genomic locations; None selected

Evidence status


Archive dbSNP rs116373211, rs116995068

HGVS name


This variation has assays on 8 chips - click the plus to show

About this variant

This variant has 2282 individual genotypes, is associated with 8 phenotypes and is mentioned in 1 citation.

Variation displays