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

This variation maps to 2 genomic locations; None selected

Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

HGVS name

None

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant has 2504 individual genotypes and is associated with 3 phenotypes.

Variation displays