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

This variation has 3 synonyms - click the plus to show

HGVS name

None

About this variant

This variant overlaps 1 transcript and is associated with 5 phenotypes.

Variation displays