rs587779411

Orientation

plus

Stabilized

plus

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

Make rs587779411(C;G)

Make rs587779411(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

8

Position

1780498

Gene

CLN8

is a	snp
is	mentioned by
dbSNP	rs587779411
dbSNP (classic)	rs587779411
ClinGen	rs587779411
ebi	rs587779411
HLI	rs587779411
Exac	rs587779411
Gnomad	rs587779411
Varsome	rs587779411
LitVar	rs587779411
Map	rs587779411
PheGenI	rs587779411
Biobank	rs587779411
1000 genomes	rs587779411
hgdp	rs587779411
ensembl	rs587779411
geneview	rs587779411
scholar	rs587779411
google	rs587779411
pharmgkb	rs587779411
gwascentral	rs587779411
openSNP	rs587779411
23andMe	rs587779411
SNPshot	rs587779411
SNPdbe	rs587779411
MSV3d	rs587779411
GWAS Ctlg	rs587779411

Max Magnitude

0

ClinVar
Risk	rs587779411(G;G)
Alt	rs587779411(G;G)
Reference	Rs587779411(C;C)
Significance	Pathogenic
Disease	Ceroid lipofuscinosis neuronal 8
Variation	info
Gene	CLN8
CLNDBN	Ceroid lipofuscinosis neuronal 8
Reversed	0
HGVS	NC_000008.10:g.1728664C>G
CLNSRC
CLNACC	RCV000087102.1, RCV000201947.1,