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]

C/T | Ambiguity code: Y | MAF: 0.07 (T)

This variation maps to 7 genomic locations; None selected

Evidence status

This variation has 19 synonyms - click the plus to show

HGVS name


About this variant

This variant has 1092 individual genotypes.

Variation displays