This variation maps to 6 locations

Select a location:
Original source

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

Alleles
T/A | Ancestral: A | Ambiguity code: W | MAF: 0.19 (T)
Location

This variation maps to 6 genomic locations; None selected

Evidence status

Synonyms
HGVS name

None

This variation has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 2588 individual genotypes, is associated with 12 phenotypes and is mentioned in 2 citations.

Variation displays