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/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

This variant has 5 synonyms - click the plus to show

HGVS name

None

About this variant

This variant has 2504 sample genotypes and is associated with 4 phenotypes.

Variant displays