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
T/G | Ancestral: T | Ambiguity code: K
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

LSDB 33022, NP_000286.3:p.ASP2ALA

HGVS name

None

About this variant

This variant is associated with 4 phenotypes and is mentioned in 1 citation.

Variant displays