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rs796053465

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796053465(-;GG)
Make rs796053465(GG;GG)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position132921361
GeneTSC1
is asnp
is mentioned by
dbSNPrs796053465
dbSNP (old)rs796053465
ClinGenrs796053465
ebirs796053465
HLIrs796053465
Exacrs796053465
Varsomers796053465
Maprs796053465
PheGenIrs796053465
Biobankrs796053465
1000 genomesrs796053465
hgdprs796053465
ensemblrs796053465
gopubmedrs796053465
geneviewrs796053465
scholarrs796053465
googlers796053465
pharmgkbrs796053465
gwascentralrs796053465
openSNPrs796053465
23andMers796053465
23andMe allrs796053465
SNP Nexus

SNPshotrs796053465
SNPdbers796053465
MSV3drs796053465
GWAS Ctlgrs796053465
Max Magnitude0
ClinVar
Risk rs796053465(GG;GG)
Alt rs796053465(GG;GG)
Reference Rs796053465(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.135796749_135796750dupCC
CLNSRC
CLNACC RCV000189865.1,