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rs796053471

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053471(-;-)
Make rs796053471(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position132905865
GeneTSC1
is asnp
is mentioned by
dbSNPrs796053471
dbSNP (old)rs796053471
ClinGenrs796053471
ebirs796053471
HLIrs796053471
Exacrs796053471
Gnomadrs796053471
Varsomers796053471
Maprs796053471
PheGenIrs796053471
Biobankrs796053471
1000 genomesrs796053471
hgdprs796053471
ensemblrs796053471
gopubmedrs796053471
geneviewrs796053471
scholarrs796053471
googlers796053471
pharmgkbrs796053471
gwascentralrs796053471
openSNPrs796053471
23andMers796053471
23andMe allrs796053471
SNP Nexus

SNPshotrs796053471
SNPdbers796053471
MSV3drs796053471
GWAS Ctlgrs796053471
Max Magnitude0
ClinVar
Risk rs796053471(-;-)
Alt rs796053471(-;-)
Reference Rs796053471(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.135781252delT
CLNSRC
CLNACC RCV000189876.1,