This variant maps to 8 locations

Select a location:
Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S|MAF: < 0.01 (C)
Location

This variant maps to 8 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

This variant has 2 synonyms - Show

HGVS name

None

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant has 2504 sample genotypes and is associated with 8 phenotypes.

Variant displays