rs863224859

Orientation

plus

Stabilized

plus

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

Make rs863224859(C;T)

Make rs863224859(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

1771266

Gene

CLN8

is a	snp
is	mentioned by
dbSNP	rs863224859
dbSNP (classic)	rs863224859
ClinGen	rs863224859
ebi	rs863224859
HLI	rs863224859
Exac	rs863224859
Gnomad	rs863224859
Varsome	rs863224859
LitVar	rs863224859
Map	rs863224859
PheGenI	rs863224859
Biobank	rs863224859
1000 genomes	rs863224859
hgdp	rs863224859
ensembl	rs863224859
geneview	rs863224859
scholar	rs863224859
google	rs863224859
pharmgkb	rs863224859
gwascentral	rs863224859
openSNP	rs863224859
23andMe	rs863224859
SNPshot	rs863224859
SNPdbe	rs863224859
MSV3d	rs863224859
GWAS Ctlg	rs863224859

Max Magnitude

0

ClinVar
Risk	rs863224859(T;T)
Alt	rs863224859(T;T)
Reference	Rs863224859(C;C)
Significance	Probable-Pathogenic
Disease	Ceroid lipofuscinosis neuronal 8
Variation	info
Gene	CLN8
CLNDBN	Ceroid lipofuscinosis neuronal 8
Reversed	0
HGVS	NC_000008.10:g.1719432C>T
CLNSRC
CLNACC	RCV000197221.1,