This variant maps to 2 locations

Select a location:
Original source

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

A/G | Ambiguity code: R

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

HGVS name


About this variant

This variant overlaps 1 regulatory feature, has 1 sample genotype and is associated with 4 phenotypes.

Variant displays