This variation maps to 9 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
C/G/T | Ancestral: C | Ambiguity code: B | MAF: 0.07 (T)
Location

This variation maps to 9 genomic locations; None selected

Evidence status

This variation has 15 synonyms - click the plus to show

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays