This variation has been flagged

Variation has more than 3 different alleles

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Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/A/C/G | Ancestral: T | Ambiguity code: N | MAF: < 0.01 (C)
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

HGVS name

None

Genotyping chips

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

About this variant

This variant has 2504 individual genotypes, is associated with 8 phenotypes and is mentioned in 9 citations.

Variation displays