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/A|Ancestral: C|Ambiguity code: M
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs1209431, rs657094

HGVS name

None

About this variant

This variant overlaps 1 regulatory feature and has 1 sample genotype.

Variant displays