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rs796053484

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053484(G;T)
Make rs796053484(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2062497
GeneTSC2
is asnp
is mentioned by
dbSNPrs796053484
ClinGenrs796053484
ebirs796053484
HLIrs796053484
Exacrs796053484
Varsomers796053484
Maprs796053484
PheGenIrs796053484
hapmaprs796053484
1000 genomesrs796053484
hgdprs796053484
ensemblrs796053484
gopubmedrs796053484
geneviewrs796053484
scholarrs796053484
googlers796053484
pharmgkbrs796053484
gwascentralrs796053484
openSNPrs796053484
23andMers796053484
23andMe allrs796053484
SNP Nexus

SNPshotrs796053484
SNPdbers796053484
MSV3drs796053484
GWAS Ctlgrs796053484
Max Magnitude0
ClinVar
Risk rs796053484(C;C) rs796053484(T;T)
Alt rs796053484(C;C) rs796053484(T;T)
Reference Rs796053484(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2112498G>T
CLNSRC
CLNACC RCV000189977.1,