rs796052355

Orientation

minus

Stabilized

minus

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

Make rs796052355(C;C)

Make rs796052355(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

68211673

Gene

CLN6

is a	snp
is	mentioned by
dbSNP	rs796052355
dbSNP (classic)	rs796052355
ClinGen	rs796052355
ebi	rs796052355
HLI	rs796052355
Exac	rs796052355
Gnomad	rs796052355
Varsome	rs796052355
LitVar	rs796052355
Map	rs796052355
PheGenI	rs796052355
Biobank	rs796052355
1000 genomes	rs796052355
hgdp	rs796052355
ensembl	rs796052355
geneview	rs796052355
scholar	rs796052355
google	rs796052355
pharmgkb	rs796052355
gwascentral	rs796052355
openSNP	rs796052355
23andMe	rs796052355
SNPshot	rs796052355
SNPdbe	rs796052355
MSV3d	rs796052355
GWAS Ctlg	rs796052355

Max Magnitude

0

ClinVar
Risk	rs796052355(C;C)
Alt	rs796052355(C;C)
Reference	Rs796052355(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CLN6
CLNDBN	not provided
Reversed	1
HGVS	NC_000015.9:g.68504011A>G
CLNSRC
CLNACC	RCV000187099.1,