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rs796053496

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053496(A;A)
Make rs796053496(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2081608
GeneTSC2
is asnp
is mentioned by
dbSNPrs796053496
ebirs796053496
HLIrs796053496
Exacrs796053496
Varsomers796053496
Maprs796053496
PheGenIrs796053496
hapmaprs796053496
1000 genomesrs796053496
hgdprs796053496
ensemblrs796053496
gopubmedrs796053496
geneviewrs796053496
scholarrs796053496
googlers796053496
pharmgkbrs796053496
gwascentralrs796053496
openSNPrs796053496
23andMers796053496
23andMe allrs796053496
SNP Nexus

SNPshotrs796053496
SNPdbers796053496
MSV3drs796053496
GWAS Ctlgrs796053496
Max Magnitude0
ClinVar
Risk rs796053496(A;A)
Alt rs796053496(A;A)
Reference rs796053496(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2131609G>A
CLNSRC
CLNACC RCV000190022.2,