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rs796053506

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796053506(-;C)
Make rs796053506(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2081722
GeneTSC2
is asnp
is mentioned by
dbSNPrs796053506
dbSNP (old)rs796053506
ClinGenrs796053506
ebirs796053506
HLIrs796053506
Exacrs796053506
Gnomadrs796053506
Varsomers796053506
Maprs796053506
PheGenIrs796053506
Biobankrs796053506
1000 genomesrs796053506
hgdprs796053506
ensemblrs796053506
gopubmedrs796053506
geneviewrs796053506
scholarrs796053506
googlers796053506
pharmgkbrs796053506
gwascentralrs796053506
openSNPrs796053506
23andMers796053506
23andMe allrs796053506
SNP Nexus

SNPshotrs796053506
SNPdbers796053506
MSV3drs796053506
GWAS Ctlgrs796053506
Max Magnitude0
ClinVar
Risk rs796053506(C;C)
Alt rs796053506(C;C)
Reference Rs796053506(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2131723dupC
CLNSRC
CLNACC RCV000190063.1,