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
A/C/G/T|Ancestral: A|Ambiguity code: N|MAF: 0.29 (G)
Location

This variant maps to 3 genomic locations; None selected

Evidence status

Synonyms
HGVS name

None

About this variant

This variant overlaps 1 regulatory feature and has 2532 sample genotypes.

Variant displays