This variant maps to 2 locations

Select a location:
Original source

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

Alleles
G/C/T | Ancestral: G | Ambiguity code: B
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

LSDB 33485, 33484

HGVS name

None

About this variant

This variant overlaps 1 regulatory feature and is associated with 8 phenotypes.

Variant displays