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rs796053483

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053483(C;G)
Make rs796053483(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2060775
GeneTSC2
is asnp
is mentioned by
dbSNPrs796053483
ebirs796053483
HLIrs796053483
Exacrs796053483
Varsomers796053483
Maprs796053483
PheGenIrs796053483
hapmaprs796053483
1000 genomesrs796053483
hgdprs796053483
ensemblrs796053483
gopubmedrs796053483
geneviewrs796053483
scholarrs796053483
googlers796053483
pharmgkbrs796053483
gwascentralrs796053483
openSNPrs796053483
23andMers796053483
23andMe allrs796053483
SNP Nexus

SNPshotrs796053483
SNPdbers796053483
MSV3drs796053483
GWAS Ctlgrs796053483
Max Magnitude0
ClinVar
Risk rs796053483(G;G)
Alt rs796053483(G;G)
Reference rs796053483(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2110776C>G
CLNSRC
CLNACC RCV000189974.2,