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rs1057523509

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057523509(G;G)
Make rs1057523509(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position2061991
GeneTSC2
is asnp
is mentioned by
dbSNPrs1057523509
dbSNP (old)rs1057523509
ClinGenrs1057523509
ebirs1057523509
HLIrs1057523509
Exacrs1057523509
Gnomadrs1057523509
Varsomers1057523509
Maprs1057523509
PheGenIrs1057523509
Biobankrs1057523509
1000 genomesrs1057523509
hgdprs1057523509
ensemblrs1057523509
gopubmedrs1057523509
geneviewrs1057523509
scholarrs1057523509
googlers1057523509
pharmgkbrs1057523509
gwascentralrs1057523509
openSNPrs1057523509
23andMers1057523509
23andMe allrs1057523509
SNPshotrs1057523509
SNPdbers1057523509
MSV3drs1057523509
GWAS Ctlgrs1057523509
Max Magnitude0
ClinVar
Risk rs1057523509(G;G)
Alt rs1057523509(G;G)
Reference Rs1057523509(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2111992T>G
CLNSRC
CLNACC RCV000430283.1,