This variation maps to 2 locations

Select a location:
Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.01 (T)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni5, Illumina_Human1M-duo

Variation displays