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rs118203687

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs118203687(G;T)
Make rs118203687(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position132901690
GeneTSC1
is asnp
is mentioned by
dbSNPrs118203687
dbSNP (old)rs118203687
ClinGenrs118203687
ebirs118203687
HLIrs118203687
Exacrs118203687
Gnomadrs118203687
Varsomers118203687
LitVarrs118203687
Maprs118203687
PheGenIrs118203687
Biobankrs118203687
1000 genomesrs118203687
hgdprs118203687
ensemblrs118203687
gopubmedrs118203687
geneviewrs118203687
scholarrs118203687
googlers118203687
pharmgkbrs118203687
gwascentralrs118203687
openSNPrs118203687
23andMers118203687
23andMe allrs118203687
SNPshotrs118203687
SNPdbers118203687
MSV3drs118203687
GWAS Ctlgrs118203687
Max Magnitude0
ClinVar
Risk rs118203687(T;T)
Alt rs118203687(T;T)
Reference Rs118203687(G;G)
Significance Pathogenic
Disease Tuberous sclerosis syndrome not provided
Variation info
Gene TSC1
CLNDBN Tuberous sclerosis syndrome not provided
Reversed 1
HGVS NC_000009.11:g.135777077C>A
CLNSRC Tuberous sclerosis database (TSC1)
CLNACC RCV000042200.2, RCV000481095.1,