rs786205065

Orientation

minus

Stabilized

minus

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

Make rs786205065(-;-)

Make rs786205065(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

68229578

Gene

CLN6

is a	snp
is	mentioned by
dbSNP	rs786205065
dbSNP (classic)	rs786205065
ClinGen	rs786205065
ebi	rs786205065
HLI	rs786205065
Exac	rs786205065
Gnomad	rs786205065
Varsome	rs786205065
LitVar	rs786205065
Map	rs786205065
PheGenI	rs786205065
Biobank	rs786205065
1000 genomes	rs786205065
hgdp	rs786205065
ensembl	rs786205065
geneview	rs786205065
scholar	rs786205065
google	rs786205065
pharmgkb	rs786205065
gwascentral	rs786205065
openSNP	rs786205065
23andMe	rs786205065
SNPshot	rs786205065
SNPdbe	rs786205065
MSV3d	rs786205065
GWAS Ctlg	rs786205065

Max Magnitude

0

ClinVar
Risk	rs786205065(-;-)
Alt	rs786205065(-;-)
Reference	Rs786205065(G;G)
Significance	Pathogenic
Disease	Ceroid lipofuscinosis neuronal 6
Variation	info
Gene	CLN6
CLNDBN	Ceroid lipofuscinosis neuronal 6
Reversed	1
HGVS	NC_000015.9:g.68521916delC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004295.4,