rs690016566

Orientation

minus

Stabilized

minus

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

Make rs690016566(A;A)

Make rs690016566(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

150057312

Gene

CSF1R

is a	snp
is	mentioned by
dbSNP	rs690016566
dbSNP (classic)	rs690016566
ClinGen	rs690016566
ebi	rs690016566
HLI	rs690016566
Exac	rs690016566
Gnomad	rs690016566
Varsome	rs690016566
LitVar	rs690016566
Map	rs690016566
PheGenI	rs690016566
Biobank	rs690016566
1000 genomes	rs690016566
hgdp	rs690016566
ensembl	rs690016566
geneview	rs690016566
scholar	rs690016566
google	rs690016566
pharmgkb	rs690016566
gwascentral	rs690016566
openSNP	rs690016566
23andMe	rs690016566
SNPshot	rs690016566
SNPdbe	rs690016566
MSV3d	rs690016566
GWAS Ctlg	rs690016566

Max Magnitude

0

ClinVar
Risk	rs690016566(A;A)
Alt	rs690016566(A;A)
Reference	Rs690016566(G;G)
Significance	Pathogenic
Disease	Hereditary diffuse leukoencephalopathy with spheroids
Variation	info
Gene	CSF1R
CLNDBN	Hereditary diffuse leukoencephalopathy with spheroids
Reversed	1
HGVS	NC_000005.9:g.149436875C>T
CLNSRC
CLNACC	RCV000149542.1,