This variant has been flagged

None of the variant alleles match the reference allele

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Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/T|Ancestral: C|Ambiguity code: Y
Location

This variant maps to 7 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

This variant has 3 synonyms - Show

HGVS name

None

Genotyping chips

This variant has assays on: HumanCoreExome-12

About this variant

This variant is associated with 14 phenotypes and is mentioned in 1 citation.

Variant displays