This variation maps to 2 locations

Select a location:
Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.41 (A)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Clinical significance

HGVS name

None

This variation has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 2585 individual genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variation displays