rs104894001

Orientation

minus

Stabilized

minus

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

Make rs104894001(A;A)

Make rs104894001(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

41161522

Gene	LOC105375056, TREM2

is a	snp
is	mentioned by
dbSNP	rs104894001
dbSNP (classic)	rs104894001
ClinGen	rs104894001
ebi	rs104894001
HLI	rs104894001
Exac	rs104894001
Gnomad	rs104894001
Varsome	rs104894001
LitVar	rs104894001
Map	rs104894001
PheGenI	rs104894001
Biobank	rs104894001
1000 genomes	rs104894001
hgdp	rs104894001
ensembl	rs104894001
geneview	rs104894001
scholar	rs104894001
google	rs104894001
pharmgkb	rs104894001
gwascentral	rs104894001
openSNP	rs104894001
23andMe	rs104894001
SNPshot	rs104894001
SNPdbe	rs104894001
MSV3d	rs104894001
GWAS Ctlg	rs104894001

Max Magnitude

0

OMIM	605086
Desc
Variant	0005
Related	also

ClinVar
Risk	rs104894001(A;A)
Alt	rs104894001(A;A)
Reference	Rs104894001(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.41129260C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005527.2,