rs104893998

Orientation

minus

Stabilized

minus

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

Make rs104893998(A;A)

Make rs104893998(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

41161421

Gene	LOC105375056, TREM2

is a	snp
is	mentioned by
dbSNP	rs104893998
dbSNP (classic)	rs104893998
ClinGen	rs104893998
ebi	rs104893998
HLI	rs104893998
Exac	rs104893998
Gnomad	rs104893998
Varsome	rs104893998
LitVar	rs104893998
Map	rs104893998
PheGenI	rs104893998
Biobank	rs104893998
1000 genomes	rs104893998
hgdp	rs104893998
ensembl	rs104893998
geneview	rs104893998
scholar	rs104893998
google	rs104893998
pharmgkb	rs104893998
gwascentral	rs104893998
openSNP	rs104893998
23andMe	rs104893998
SNPshot	rs104893998
SNPdbe	rs104893998
MSV3d	rs104893998
GWAS Ctlg	rs104893998

GMAF

0.0004591

Max Magnitude

0

OMIM	605086
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104893998(A;A)
Alt	rs104893998(A;A)
Reference	Rs104893998(G;G)
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.41129159C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005523.2,