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]

G/C/T | Ambiguity code: B | MAF: 0.34 (G)

This variation maps to 7 genomic locations; None selected

Evidence status

This variation has 11 synonyms - click the plus to show

HGVS name


Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni1-Quad

About this variant

This variant has 1095 individual genotypes.

Variation displays