This variant has been flagged

None of the variant alleles match the reference allele

Select a location:
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 7 genomic locations; None selected

Evidence status

HGVS name

None

About this variant

This variant has 165 sample genotypes.

Variant displays