rs786205509

Orientation

plus

Stabilized

plus

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

Make rs786205509(C;T)

Make rs786205509(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

65190194

Gene

RGS9

is a	snp
is	mentioned by
dbSNP	rs786205509
dbSNP (classic)	rs786205509
ClinGen	rs786205509
ebi	rs786205509
HLI	rs786205509
Exac	rs786205509
Gnomad	rs786205509
Varsome	rs786205509
LitVar	rs786205509
Map	rs786205509
PheGenI	rs786205509
Biobank	rs786205509
1000 genomes	rs786205509
hgdp	rs786205509
ensembl	rs786205509
geneview	rs786205509
scholar	rs786205509
google	rs786205509
pharmgkb	rs786205509
gwascentral	rs786205509
openSNP	rs786205509
23andMe	rs786205509
SNPshot	rs786205509
SNPdbe	rs786205509
MSV3d	rs786205509
GWAS Ctlg	rs786205509

Max Magnitude

0

ClinVar
Risk	rs786205509(T;T)
Alt	rs786205509(T;T)
Reference	Rs786205509(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	RGS9
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.63186312C>T
CLNSRC
CLNACC	RCV000171265.1,