This variation maps to 8 locations

Select a location:
Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.34 (A)
Location

This variation maps to 8 genomic locations; None selected

Evidence status

HGVS name

None

This variation has assays on 11 chips - click the plus to show

About this variant

This variant has 2561 individual genotypes, is associated with 8 phenotypes and is mentioned in 1 citation.

Variation displays