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rs796053517

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053517(-;-)
Make rs796053517(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2081723
GeneTSC2
is asnp
is mentioned by
dbSNPrs796053517
dbSNP (old)rs796053517
ClinGenrs796053517
ebirs796053517
HLIrs796053517
Exacrs796053517
Gnomadrs796053517
Varsomers796053517
Maprs796053517
PheGenIrs796053517
Biobankrs796053517
1000 genomesrs796053517
hgdprs796053517
ensemblrs796053517
gopubmedrs796053517
geneviewrs796053517
scholarrs796053517
googlers796053517
pharmgkbrs796053517
gwascentralrs796053517
openSNPrs796053517
23andMers796053517
23andMe allrs796053517
SNP Nexus

SNPshotrs796053517
SNPdbers796053517
MSV3drs796053517
GWAS Ctlgrs796053517
Max Magnitude0
ClinVar
Risk rs796053517(-;-)
Alt rs796053517(-;-)
Reference Rs796053517(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2131724delA
CLNSRC
CLNACC RCV000190086.1,