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|MAF: < 0.01 (T)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

LSDB 12414

HGVS name

None

About this variant

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

Variant displays