rs796052351

Orientation

minus

Stabilized

minus

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

Make rs796052351(A;A)

Make rs796052351(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

68214289

Gene

CLN6

is a	snp
is	mentioned by
dbSNP	rs796052351
dbSNP (classic)	rs796052351
ClinGen	rs796052351
ebi	rs796052351
HLI	rs796052351
Exac	rs796052351
Gnomad	rs796052351
Varsome	rs796052351
LitVar	rs796052351
Map	rs796052351
PheGenI	rs796052351
Biobank	rs796052351
1000 genomes	rs796052351
hgdp	rs796052351
ensembl	rs796052351
geneview	rs796052351
scholar	rs796052351
google	rs796052351
pharmgkb	rs796052351
gwascentral	rs796052351
openSNP	rs796052351
23andMe	rs796052351
SNPshot	rs796052351
SNPdbe	rs796052351
MSV3d	rs796052351
GWAS Ctlg	rs796052351

Max Magnitude

0

ClinVar
Risk	rs796052351(A;A)
Alt	rs796052351(A;A)
Reference	Rs796052351(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CLN6
CLNDBN	not provided
Reversed	1
HGVS	NC_000015.9:g.68506627C>T
CLNSRC
CLNACC	RCV000187092.1,