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rs796053504

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796053504(-;C)
Make rs796053504(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2077619
GeneTSC2
is asnp
is mentioned by
dbSNPrs796053504
dbSNP (old)rs796053504
ClinGenrs796053504
ebirs796053504
HLIrs796053504
Exacrs796053504
Gnomadrs796053504
Varsomers796053504
Maprs796053504
PheGenIrs796053504
Biobankrs796053504
1000 genomesrs796053504
hgdprs796053504
ensemblrs796053504
gopubmedrs796053504
geneviewrs796053504
scholarrs796053504
googlers796053504
pharmgkbrs796053504
gwascentralrs796053504
openSNPrs796053504
23andMers796053504
23andMe allrs796053504
SNP Nexus

SNPshotrs796053504
SNPdbers796053504
MSV3drs796053504
GWAS Ctlgrs796053504
Max Magnitude0
ClinVar
Risk rs796053504(C;C)
Alt rs796053504(C;C)
Reference Rs796053504(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2127620dupC
CLNSRC
CLNACC RCV000190060.1,