This variation maps to 5 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.20 (C)
Location

This variation maps to 5 genomic locations; None selected

Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

HGVS name

None

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_HumanOmni5

About this variant

This variant has 2504 individual genotypes, is associated with 13 phenotypes and is mentioned in 7 citations.

Variation displays