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

rs137854155

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854155(C;T)
Make rs137854155(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2076094
GeneTSC2
is asnp
is mentioned by
dbSNPrs137854155
ebirs137854155
HLIrs137854155
Exacrs137854155
Varsomers137854155
Maprs137854155
PheGenIrs137854155
hapmaprs137854155
1000 genomesrs137854155
hgdprs137854155
ensemblrs137854155
gopubmedrs137854155
geneviewrs137854155
scholarrs137854155
googlers137854155
pharmgkbrs137854155
gwascentralrs137854155
openSNPrs137854155
23andMers137854155
23andMe allrs137854155
SNP Nexus

SNPshotrs137854155
SNPdbers137854155
MSV3drs137854155
GWAS Ctlgrs137854155
Max Magnitude0
ClinVar
Risk rs137854155(T;T)
Alt rs137854155(T;T)
Reference rs137854155(C;C)
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.2126095C>T
CLNSRC Tuberous sclerosis database (TSC2)
CLNACC RCV000042847.2, RCV000201152.1,