This variant maps to 2 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/T|Ancestral: C|Ambiguity code: Y
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

This variant has 2 synonyms - Show

HGVS name

None

About this variant

This variant overlaps 1 regulatory feature, is associated with 8 phenotypes and is mentioned in 1 citation.

Variant displays