rs782392706

Orientation

plus

Stabilized

plus

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

Make rs782392706(C;G)

Make rs782392706(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

41769480

Gene

JUP

is a	snp
is	mentioned by
dbSNP	rs782392706
dbSNP (classic)	rs782392706
ClinGen	rs782392706
ebi	rs782392706
HLI	rs782392706
Exac	rs782392706
Gnomad	rs782392706
Varsome	rs782392706
LitVar	rs782392706
Map	rs782392706
PheGenI	rs782392706
Biobank	rs782392706
1000 genomes	rs782392706
hgdp	rs782392706
ensembl	rs782392706
geneview	rs782392706
scholar	rs782392706
google	rs782392706
pharmgkb	rs782392706
gwascentral	rs782392706
openSNP	rs782392706
23andMe	rs782392706
SNPshot	rs782392706
SNPdbe	rs782392706
MSV3d	rs782392706
GWAS Ctlg	rs782392706

Merged from

Rs794729032

Max Magnitude

0

ClinVar
Risk	rs782392706(G;G) rs782392706(T;T)
Alt	rs782392706(G;G) rs782392706(T;T)
Reference	Rs782392706(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	JUP
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.39925732C>G
CLNSRC
CLNACC	RCV000183484.2,