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rs759183842

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs759183842(C;C)
Make rs759183842(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position132925736
GeneTSC1
is asnp
is mentioned by
dbSNPrs759183842
ebirs759183842
HLIrs759183842
Exacrs759183842
Varsomers759183842
Maprs759183842
PheGenIrs759183842
hapmaprs759183842
1000 genomesrs759183842
hgdprs759183842
ensemblrs759183842
gopubmedrs759183842
geneviewrs759183842
scholarrs759183842
googlers759183842
pharmgkbrs759183842
gwascentralrs759183842
openSNPrs759183842
23andMers759183842
23andMe allrs759183842
SNP Nexus

SNPshotrs759183842
SNPdbers759183842
MSV3drs759183842
GWAS Ctlgrs759183842
Max Magnitude0
ClinVar
Risk rs759183842(A,C;A,C)
Alt rs759183842(A,C;A,C)
Reference rs759183842(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TSC1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.135801123G>C
CLNSRC
CLNACC RCV000189832.1,