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
A/C | Ancestral: A | Ambiguity code: M
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

This variant has 4 synonyms - click the plus to show

HGVS name

None

About this variant

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

Variant displays