rs786205066

Orientation

minus

Stabilized

minus

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

Make rs786205066(G;T)

Make rs786205066(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

68211258

Gene

CLN6

is a	snp
is	mentioned by
dbSNP	rs786205066
dbSNP (classic)	rs786205066
ClinGen	rs786205066
ebi	rs786205066
HLI	rs786205066
Exac	rs786205066
Gnomad	rs786205066
Varsome	rs786205066
LitVar	rs786205066
Map	rs786205066
PheGenI	rs786205066
Biobank	rs786205066
1000 genomes	rs786205066
hgdp	rs786205066
ensembl	rs786205066
geneview	rs786205066
scholar	rs786205066
google	rs786205066
pharmgkb	rs786205066
gwascentral	rs786205066
openSNP	rs786205066
23andMe	rs786205066
SNPshot	rs786205066
SNPdbe	rs786205066
MSV3d	rs786205066
GWAS Ctlg	rs786205066

Max Magnitude

0

ClinVar
Risk	rs786205066(T;T)
Alt	rs786205066(T;T)
Reference	Rs786205066(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.68503596C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004300.4,