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rs121908402

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908402(G;G)
Make rs121908402(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position41161277
GeneTREM2
is asnp
is mentioned by
dbSNPrs121908402
ebirs121908402
HLIrs121908402
Exacrs121908402
Varsomers121908402
Maprs121908402
PheGenIrs121908402
hapmaprs121908402
1000 genomesrs121908402
hgdprs121908402
ensemblrs121908402
gopubmedrs121908402
geneviewrs121908402
scholarrs121908402
googlers121908402
pharmgkbrs121908402
gwascentralrs121908402
openSNPrs121908402
23andMers121908402
23andMe allrs121908402
SNP Nexus

SNPshotrs121908402
SNPdbers121908402
MSV3drs121908402
GWAS Ctlgrs121908402
Max Magnitude0
OMIM605086
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121908402(G;G)
Alt rs121908402(G;G)
Reference rs121908402(T;T)
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.41129015A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000005528.2,