Original source

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

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

Chromosome 8:118933071 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM034979

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 11321, 2010_April_001_062_TNFRSF11B_602643_0003

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and is associated with 2 phenotypes.

Variant displays