This variation maps to 2 locations

Select a location:
Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.31 (A)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

HGVS name

None

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

About this variant

This variant has 3910 individual genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variation displays