This variation 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

G/A/C/T | Ambiguity code: N

This variation maps to 7 genomic locations; None selected

Evidence status

This variation has 6 synonyms - click the plus to show

HGVS name


About this variant

This variant has 2 individual genotypes.

Variation displays