This variant has been flagged

Variation has more than 3 different alleles

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Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A/C/T|Ancestral: G|Ambiguity code: N|MAF: < 0.01 (C)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

HGVS name

None

About this variant

This variant has 2504 sample genotypes.

Variant displays