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
A/C|Ambiguity code: M|MAF: 0.42 (C)
Location

This variant maps to 7 genomic locations; None selected

Evidence status

HGVS name

None

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 1 regulatory feature, has 2508 sample genotypes and is mentioned in 1 citation.

Variant displays