rs201258663

Orientation

plus

Stabilized

plus

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

Make rs201258663(A;A)

Make rs201258663(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

41161457

Gene	LOC105375056, TREM2

is a	snp
is	mentioned by
dbSNP	rs201258663
dbSNP (classic)	rs201258663
ClinGen	rs201258663
ebi	rs201258663
HLI	rs201258663
Exac	rs201258663
Gnomad	rs201258663
Varsome	rs201258663
LitVar	rs201258663
Map	rs201258663
PheGenI	rs201258663
Biobank	rs201258663
1000 genomes	rs201258663
hgdp	rs201258663
ensembl	rs201258663
geneview	rs201258663
scholar	rs201258663
google	rs201258663
pharmgkb	rs201258663
gwascentral	rs201258663
openSNP	rs201258663
23andMe	rs201258663
SNPshot	rs201258663
SNPdbe	rs201258663
MSV3d	rs201258663
GWAS Ctlg	rs201258663

Max Magnitude

0

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,