This variation maps to 12 locations

Select a location:
Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

This variation maps to 12 genomic locations; None selected

Evidence status

This variation has 11 synonyms - click the plus to show

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant has 9 individual genotypes.

Variation displays