rs386834141

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs386834141(-;-)

Make rs386834141(-;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

41161341

Gene	LOC105375056, TREM2

is a	snp
is	mentioned by
dbSNP	rs386834141
dbSNP (classic)	rs386834141
ClinGen	rs386834141
ebi	rs386834141
HLI	rs386834141
Exac	rs386834141
Gnomad	rs386834141
Varsome	rs386834141
LitVar	rs386834141
Map	rs386834141
PheGenI	rs386834141
Biobank	rs386834141
1000 genomes	rs386834141
hgdp	rs386834141
ensembl	rs386834141
geneview	rs386834141
scholar	rs386834141
google	rs386834141
pharmgkb	rs386834141
gwascentral	rs386834141
openSNP	rs386834141
23andMe	rs386834141
SNPshot	rs386834141
SNPdbe	rs386834141
MSV3d	rs386834141
GWAS Ctlg	rs386834141

Max Magnitude

0

ClinVar
Risk	rs386834141(-;-)
Alt	rs386834141(-;-)
Reference	Rs386834141(G;G)
Significance	Probable-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.41129079delC
CLNSRC	ClinVar
CLNACC	RCV000050135.1,

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