rs794729032

Merged into

rs782392706

Orientation

minus

Stabilized

minus

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

Make rs794729032(C;C)

Make rs794729032(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

41769480

Gene

JUP

is a	snp
is	mentioned by
dbSNP	rs794729032
dbSNP (classic)	rs794729032
ClinGen	rs794729032
ebi	rs794729032
HLI	rs794729032
Exac	rs794729032
Gnomad	rs794729032
Varsome	rs794729032
LitVar	rs794729032
Map	rs794729032
PheGenI	rs794729032
Biobank	rs794729032
1000 genomes	rs794729032
hgdp	rs794729032
ensembl	rs794729032
geneview	rs794729032
scholar	rs794729032
google	rs794729032
pharmgkb	rs794729032
gwascentral	rs794729032
openSNP	rs794729032
23andMe	rs794729032
SNPshot	rs794729032
SNPdbe	rs794729032
MSV3d	rs794729032
GWAS Ctlg	rs794729032

Status

Merged into rs782392706

Max Magnitude

0

ClinVar
Risk	rs794729032(C;C)
Alt	rs794729032(C;C)
Reference	Rs794729032(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	JUP
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.39925732C>G
CLNSRC
CLNACC	RCV000183484.2,