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rs796053470

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796053470(-;T)
Make rs796053470(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position132906068
GeneTSC1
is asnp
is mentioned by
dbSNPrs796053470
ClinGenrs796053470
ebirs796053470
HLIrs796053470
Exacrs796053470
Varsomers796053470
Maprs796053470
PheGenIrs796053470
hapmaprs796053470
1000 genomesrs796053470
hgdprs796053470
ensemblrs796053470
gopubmedrs796053470
geneviewrs796053470
scholarrs796053470
googlers796053470
pharmgkbrs796053470
gwascentralrs796053470
openSNPrs796053470
23andMers796053470
23andMe allrs796053470
SNP Nexus

SNPshotrs796053470
SNPdbers796053470
MSV3drs796053470
GWAS Ctlgrs796053470
Max Magnitude0
ClinVar
Risk rs796053470(T;T)
Alt rs796053470(T;T)
Reference Rs796053470(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.135781456dupA
CLNSRC
CLNACC RCV000189875.1,