This variation maps to 7 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: T | Ambiguity code: W | MAF: 0.04 (A)
Location

This variation maps to 7 genomic locations; None selected

Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

HGVS name

None

This variation has assays on 6 chips - click the plus to show

About this variant

This variant has 1470 individual genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variation displays