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 142) | View in dbSNP

C/A/G/T | Ambiguity code: N | MAF: 0.02 (A)

This variant maps to 7 genomic locations; None selected

Evidence status

This variant has 2 synonyms - click the plus to show

HGVS name


About this variant

This variant has 2505 sample genotypes.

Variant displays