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rs28937876

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
(T;T) 2
Make rs28937876(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position41158991
GeneTREM2
is asnp
is mentioned by
dbSNPrs28937876
ebirs28937876
HLIrs28937876
Exacrs28937876
Varsomers28937876
Maprs28937876
PheGenIrs28937876
hapmaprs28937876
1000 genomesrs28937876
hgdprs28937876
ensemblrs28937876
gopubmedrs28937876
geneviewrs28937876
scholarrs28937876
googlers28937876
pharmgkbrs28937876
gwascentralrs28937876
openSNPrs28937876
23andMers28937876
23andMe allrs28937876
SNP Nexus

SNPshotrs28937876
SNPdbers28937876
MSV3drs28937876
GWAS Ctlgrs28937876
Max Magnitude2
OMIM605086
DescPOLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY
Variant0002
Relatedalso
Neighborrs28939079
Distance882


ClinVar
Risk rs28937876(T;T)
Alt rs28937876(T;T)
Reference rs28937876(G;G)
Significance Pathogenic
Disease Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
Variation info
Gene TREM2
CLNDBN Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
Reversed 1
HGVS NC_000006.11:g.41126729C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005524.2,