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rs137854261

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAG;AAG) 0 common in clinvar
(GAA;GAA) 0 common in clinvar
Make rs137854261(-;-)
Make rs137854261(-;GAA)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2086793
GeneTSC2
is asnp
is mentioned by
dbSNPrs137854261
dbSNP (old)rs137854261
ClinGenrs137854261
ebirs137854261
HLIrs137854261
Exacrs137854261
Gnomadrs137854261
Varsomers137854261
Maprs137854261
PheGenIrs137854261
Biobankrs137854261
1000 genomesrs137854261
hgdprs137854261
ensemblrs137854261
gopubmedrs137854261
geneviewrs137854261
scholarrs137854261
googlers137854261
pharmgkbrs137854261
gwascentralrs137854261
openSNPrs137854261
23andMers137854261
23andMe allrs137854261
SNP Nexus

SNPshotrs137854261
SNPdbers137854261
MSV3drs137854261
GWAS Ctlgrs137854261
Merged fromRs137854290
Max Magnitude0
ClinVar
Risk rs137854261(-;-) Rs137854261(AAG;AAG)
Alt rs137854261(-;-) Rs137854261(AAG;AAG)
Reference Rs137854261(GAA;GAA)
Significance Pathogenic
Disease Tuberous sclerosis syndrome Tuberous sclerosis 2
Variation info
Gene TSC2
CLNDBN Tuberous sclerosis syndrome Tuberous sclerosis 2
Reversed 0
HGVS NC_000016.9:g.2136795_2136797delAAG
CLNSRC Tuberous sclerosis database (TSC2)
CLNACC RCV000043159.3, RCV000201053.1,