Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R
Location

Chromosome 8:118932982 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM034980

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 11322, 2010_April_001_063_TNFRSF11B_602643_0004

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