This variation maps to 2 locations

Select a location:
Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

This variation maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

LSDB NP_000286.3:p.PRO369LEU, 33004

HGVS name

None

Genotyping chips

This variation has assays on: HumanCoreExome-12

About this variant

This variant is associated with 3 phenotypes and is mentioned in 1 citation.

Variation displays