Have questions? Visit https://www.reddit.com/r/SNPedia

rs796053505

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796053505(-;T)
Make rs796053505(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2081781
GeneTSC2
is asnp
is mentioned by
dbSNPrs796053505
dbSNP (old)rs796053505
ClinGenrs796053505
ebirs796053505
HLIrs796053505
Exacrs796053505
Varsomers796053505
Maprs796053505
PheGenIrs796053505
Biobankrs796053505
1000 genomesrs796053505
hgdprs796053505
ensemblrs796053505
gopubmedrs796053505
geneviewrs796053505
scholarrs796053505
googlers796053505
pharmgkbrs796053505
gwascentralrs796053505
openSNPrs796053505
23andMers796053505
23andMe allrs796053505
SNP Nexus

SNPshotrs796053505
SNPdbers796053505
MSV3drs796053505
GWAS Ctlgrs796053505
Max Magnitude0
ClinVar
Risk rs796053505(T;T)
Alt rs796053505(T;T)
Reference Rs796053505(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2131782dupT
CLNSRC
CLNACC RCV000190062.1,