This variant maps to 2 locations

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Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

This variant maps to 2 genomic locations; None selected

Evidence status

This variant has 4 synonyms - click the plus to show

HGVS name


About this variant

This variant has 2 sample genotypes.

Variant displays