This variant 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 144) | View in dbSNP

C/A/G/T | Ancestral: C | Ambiguity code: N

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance


This variant has 5 synonyms - Show

HGVS name


Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 1 regulatory feature and is associated with 6 phenotypes.

Variant displays