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rs796051868

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GAC;GAC) 0 common in clinvar
Make rs796051868(-;-)
Make rs796051868(-;GAC)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position118928784
GeneTNFRSF11B
is asnp
is mentioned by
dbSNPrs796051868
ClinGenrs796051868
ebirs796051868
HLIrs796051868
Exacrs796051868
Varsomers796051868
Maprs796051868
PheGenIrs796051868
hapmaprs796051868
1000 genomesrs796051868
hgdprs796051868
ensemblrs796051868
gopubmedrs796051868
geneviewrs796051868
scholarrs796051868
googlers796051868
pharmgkbrs796051868
gwascentralrs796051868
openSNPrs796051868
23andMers796051868
23andMe allrs796051868
SNP Nexus

SNPshotrs796051868
SNPdbers796051868
MSV3drs796051868
GWAS Ctlgrs796051868
Max Magnitude0
ClinVar
Risk rs796051868(-;-)
Alt rs796051868(-;-)
Reference Rs796051868(GAC;GAC)
Significance Pathogenic
Disease Hyperphosphatasemia with bone disease
Variation info
Gene TNFRSF11B
CLNDBN Hyperphosphatasemia with bone disease
Reversed 1
HGVS NC_000008.10:g.119941023_119941025delGTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000007384.5,