rs797044603

Orientation

minus

Stabilized

minus

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

Make rs797044603(A;G)

Make rs797044603(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

41161541

Gene	LOC105375056, TREM2

is a	snp
is	mentioned by
dbSNP	rs797044603
dbSNP (classic)	rs797044603
ClinGen	rs797044603
ebi	rs797044603
HLI	rs797044603
Exac	rs797044603
Gnomad	rs797044603
Varsome	rs797044603
LitVar	rs797044603
Map	rs797044603
PheGenI	rs797044603
Biobank	rs797044603
1000 genomes	rs797044603
hgdp	rs797044603
ensembl	rs797044603
geneview	rs797044603
scholar	rs797044603
google	rs797044603
pharmgkb	rs797044603
gwascentral	rs797044603
openSNP	rs797044603
23andMe	rs797044603
SNPshot	rs797044603
SNPdbe	rs797044603
MSV3d	rs797044603
GWAS Ctlg	rs797044603

Max Magnitude

0

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,