This variation has been flagged

Variation maps to 3 genomic locations

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Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

A/G | Ancestral: G | Ambiguity code: R

This variation maps to 3 genomic locations; None selected

Evidence status

This variation has 2 synonyms - click the plus to show

HGVS name


Variation displays