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

This variant maps to 2 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: Illumina_Human1M-duo, Illumina_ExomeChip, Illumina_HumanOmni5

About this variant

This variant has 2994 sample genotypes, is associated with 8 phenotypes and is mentioned in 1 citation.

Variant displays