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rs201258663

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201258663(A;A)
Make rs201258663(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position41161457
GeneLOC105375056, TREM2
is asnp
is mentioned by
dbSNPrs201258663
ebirs201258663
HLIrs201258663
Exacrs201258663
Varsomers201258663
Maprs201258663
PheGenIrs201258663
hapmaprs201258663
1000 genomesrs201258663
hgdprs201258663
ensemblrs201258663
gopubmedrs201258663
geneviewrs201258663
scholarrs201258663
googlers201258663
pharmgkbrs201258663
gwascentralrs201258663
openSNPrs201258663
23andMers201258663
23andMe allrs201258663
SNP Nexus

SNPshotrs201258663
SNPdbers201258663
MSV3drs201258663
GWAS Ctlgrs201258663
Max Magnitude0
ClinVar
Risk rs201258663(A;A)
Alt rs201258663(A;A)
Reference rs201258663(G;G)
Significance Pathogenic
Disease Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
Variation info
Gene TREM2
CLNDBN Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
Reversed 0
HGVS NC_000006.11:g.41129195G>A
CLNSRC
CLNACC RCV000192213.1,