This variation maps to 7 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/A | Ambiguity code: M | MAF: 0.10 (A)
Location

This variation maps to 7 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs1048263, rs3188280, rs2308886

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant has 2505 individual genotypes.

Variation displays