This variation maps to 2 locations

Select a location:
Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

About this variant

This variant has 2 individual genotypes, is associated with 12 phenotypes and is mentioned in 1 citation.

Variation displays