This variation maps to 10 locations

Select a location:
Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: < 0.01 (G)
Location

This variation maps to 10 genomic locations; None selected

Evidence status

HGVS name

None

About this variant

This variant has 1096 individual genotypes.

Variation displays