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/G|Ambiguity code: V|MAF: 0.14 (G)
Location

This variant maps to 5 genomic locations; None selected

Evidence status

Synonyms

This variant has 19 synonyms - Show

HGVS name

None

About this variant

This variant overlaps 1 regulatory feature and has 2507 sample genotypes.

Variant displays