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rs797044603

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044603(A;G)
Make rs797044603(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position41161541
GeneLOC105375056, TREM2
is asnp
is mentioned by
dbSNPrs797044603
ebirs797044603
HLIrs797044603
Exacrs797044603
Varsomers797044603
Maprs797044603
PheGenIrs797044603
hapmaprs797044603
1000 genomesrs797044603
hgdprs797044603
ensemblrs797044603
gopubmedrs797044603
geneviewrs797044603
scholarrs797044603
googlers797044603
pharmgkbrs797044603
gwascentralrs797044603
openSNPrs797044603
23andMers797044603
23andMe allrs797044603
SNP Nexus

SNPshotrs797044603
SNPdbers797044603
MSV3drs797044603
GWAS Ctlgrs797044603
Max Magnitude0
ClinVar
Risk rs797044603(G;G)
Alt rs797044603(G;G)
Reference rs797044603(A;A)
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.41129279T>C
CLNSRC
CLNACC RCV000192212.1,