This variant maps to 2 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/C/G|Ambiguity code: V
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

This variant has 8 synonyms - Show

HGVS name

None

About this variant

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

Variant displays