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rs118203631

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs118203631(C;T)
Make rs118203631(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position132903785
GeneTSC1
is asnp
is mentioned by
dbSNPrs118203631
ebirs118203631
HLIrs118203631
Exacrs118203631
Varsomers118203631
Maprs118203631
PheGenIrs118203631
hapmaprs118203631
1000 genomesrs118203631
hgdprs118203631
ensemblrs118203631
gopubmedrs118203631
geneviewrs118203631
scholarrs118203631
googlers118203631
pharmgkbrs118203631
gwascentralrs118203631
openSNPrs118203631
23andMers118203631
23andMe allrs118203631
SNP Nexus

SNPshotrs118203631
SNPdbers118203631
MSV3drs118203631
GWAS Ctlgrs118203631
Max Magnitude0
ClinVar
Risk rs118203631(T;T)
Alt rs118203631(T;T)
Reference rs118203631(C;C)
Significance Pathogenic
Disease Tuberous sclerosis syndrome Malignant tumor of urinary bladder Tuberous sclerosis 1
Variation info
Gene TSC1
CLNDBN Tuberous sclerosis syndrome Malignant tumor of urinary bladder Tuberous sclerosis 1
Reversed 1
HGVS NC_000009.11:g.135779172G>A
CLNSRC Tuberous sclerosis database (TSC1)
CLNACC RCV000042136.2, RCV000054891.1, RCV000201087.2,