rs121908402

Orientation

minus

Stabilized

minus

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

Make rs121908402(G;G)

Make rs121908402(G;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

41161277

Gene	LOC105375056, TREM2

is a	snp
is	mentioned by
dbSNP	rs121908402
dbSNP (classic)	rs121908402
ClinGen	rs121908402
ebi	rs121908402
HLI	rs121908402
Exac	rs121908402
Gnomad	rs121908402
Varsome	rs121908402
LitVar	rs121908402
Map	rs121908402
PheGenI	rs121908402
Biobank	rs121908402
1000 genomes	rs121908402
hgdp	rs121908402
ensembl	rs121908402
geneview	rs121908402
scholar	rs121908402
google	rs121908402
pharmgkb	rs121908402
gwascentral	rs121908402
openSNP	rs121908402
23andMe	rs121908402
SNPshot	rs121908402
SNPdbe	rs121908402
MSV3d	rs121908402
GWAS Ctlg	rs121908402

Max Magnitude

0

OMIM	605086
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121908402(G;G)
Alt	rs121908402(G;G)
Reference	Rs121908402(T;T)
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.41129015A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005528.2,