rs796052354

Orientation

minus

Stabilized

minus

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

Make rs796052354(A;G)

Make rs796052354(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

68211727

Gene

CLN6

is a	snp
is	mentioned by
dbSNP	rs796052354
dbSNP (classic)	rs796052354
ClinGen	rs796052354
ebi	rs796052354
HLI	rs796052354
Exac	rs796052354
Gnomad	rs796052354
Varsome	rs796052354
LitVar	rs796052354
Map	rs796052354
PheGenI	rs796052354
Biobank	rs796052354
1000 genomes	rs796052354
hgdp	rs796052354
ensembl	rs796052354
geneview	rs796052354
scholar	rs796052354
google	rs796052354
pharmgkb	rs796052354
gwascentral	rs796052354
openSNP	rs796052354
23andMe	rs796052354
SNPshot	rs796052354
SNPdbe	rs796052354
MSV3d	rs796052354
GWAS Ctlg	rs796052354

Max Magnitude

0

ClinVar
Risk	rs796052354(G;G)
Alt	rs796052354(G;G)
Reference	Rs796052354(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CLN6
CLNDBN	not provided
Reversed	1
HGVS	NC_000015.9:g.68504065T>C
CLNSRC
CLNACC	RCV000187098.1,