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rs137854298

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137854298(G;G)
Make rs137854298(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2061980
GeneTSC2
is asnp
is mentioned by
dbSNPrs137854298
ebirs137854298
HLIrs137854298
Exacrs137854298
Varsomers137854298
Maprs137854298
PheGenIrs137854298
hapmaprs137854298
1000 genomesrs137854298
hgdprs137854298
ensemblrs137854298
gopubmedrs137854298
geneviewrs137854298
scholarrs137854298
googlers137854298
pharmgkbrs137854298
gwascentralrs137854298
openSNPrs137854298
23andMers137854298
23andMe allrs137854298
SNP Nexus

SNPshotrs137854298
SNPdbers137854298
MSV3drs137854298
GWAS Ctlgrs137854298
Max Magnitude0
ClinVar
Risk rs137854298(G;G)
Alt rs137854298(G;G)
Reference rs137854298(T;T)
Significance Probable-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.2111981T>G
CLNSRC Tuberous sclerosis database (TSC2)
CLNACC RCV000042942.2, RCV000201010.1,