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rs786205509

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205509(C;T)
Make rs786205509(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position65190194
GeneRGS9
is asnp
is mentioned by
dbSNPrs786205509
ebirs786205509
HLIrs786205509
Exacrs786205509
Varsomers786205509
Maprs786205509
PheGenIrs786205509
hapmaprs786205509
1000 genomesrs786205509
hgdprs786205509
ensemblrs786205509
gopubmedrs786205509
geneviewrs786205509
scholarrs786205509
googlers786205509
pharmgkbrs786205509
gwascentralrs786205509
openSNPrs786205509
23andMers786205509
23andMe allrs786205509
SNP Nexus

SNPshotrs786205509
SNPdbers786205509
MSV3drs786205509
GWAS Ctlgrs786205509
Max Magnitude0
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,