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/G|Ancestral: A|Ambiguity code: R|MAF: < 0.01 (G)
Location

This variant maps to 8 genomic locations; None selected

Evidence status

HGVS name

None

About this variant

This variant overlaps 1 regulatory feature and has 2504 sample genotypes.

Variant displays