This variant maps to 2 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

This variant has 5 synonyms - Show

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

This variant has 2 sample genotypes, is associated with 20 phenotypes and is mentioned in 1 citation.

Variant displays