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rs587778729

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778729(G;T)
Make rs587778729(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2065519
GeneTSC2
is asnp
is mentioned by
dbSNPrs587778729
ebirs587778729
HLIrs587778729
Exacrs587778729
Varsomers587778729
Maprs587778729
PheGenIrs587778729
hapmaprs587778729
1000 genomesrs587778729
hgdprs587778729
ensemblrs587778729
gopubmedrs587778729
geneviewrs587778729
scholarrs587778729
googlers587778729
pharmgkbrs587778729
gwascentralrs587778729
openSNPrs587778729
23andMers587778729
23andMe allrs587778729
SNP Nexus

SNPshotrs587778729
SNPdbers587778729
MSV3drs587778729
GWAS Ctlgrs587778729
Max Magnitude0
ClinVar
Risk rs587778729(T;T)
Alt rs587778729(T;T)
Reference rs587778729(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene TSC2
CLNDBN not specified not provided
Reversed 0
HGVS NC_000016.9:g.2115520G>T
CLNSRC
CLNACC RCV000122207.1, RCV000189984.1,