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
T/C/G|Ancestral: T|Ambiguity code: B|MAF: < 0.01 (C)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

This variant has 4 synonyms - Show

HGVS name

None

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_HumanOmni1-Quad, Illumina_ExomeChip

About this variant

This variant has 2504 sample genotypes, is associated with 14 phenotypes and is mentioned in 9 citations.

Variant displays