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rs386833841

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs386833841(C;C)
Make rs386833841(C;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position35907530
GeneTYROBP
is asnp
is mentioned by
dbSNPrs386833841
ebirs386833841
HLIrs386833841
Exacrs386833841
Varsomers386833841
Maprs386833841
PheGenIrs386833841
hapmaprs386833841
1000 genomesrs386833841
hgdprs386833841
ensemblrs386833841
gopubmedrs386833841
geneviewrs386833841
scholarrs386833841
googlers386833841
pharmgkbrs386833841
gwascentralrs386833841
openSNPrs386833841
23andMers386833841
23andMe allrs386833841
SNP Nexus

SNPshotrs386833841
SNPdbers386833841
MSV3drs386833841
GWAS Ctlgrs386833841
Max Magnitude0
ClinVar
Risk rs386833841(C;C)
Alt rs386833841(C;C)
Reference rs386833841(G;G)
Significance Probable-Pathogenic
Disease Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
Variation info
Gene TYROBP
CLNDBN Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
Reversed 1
HGVS NC_000019.9:g.36398432C>G
CLNSRC ClinVar
CLNACC RCV000049809.1,


[PMID 15883308] The genetic causes of basal ganglia calcification, dementia, and bone cysts: DAP12 and TREM2.