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rs118203606

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs118203606(C;T)
Make rs118203606(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position132905615
GeneTSC1
is asnp
is mentioned by
dbSNPrs118203606
ebirs118203606
HLIrs118203606
Exacrs118203606
Varsomers118203606
Maprs118203606
PheGenIrs118203606
hapmaprs118203606
1000 genomesrs118203606
hgdprs118203606
ensemblrs118203606
gopubmedrs118203606
geneviewrs118203606
scholarrs118203606
googlers118203606
pharmgkbrs118203606
gwascentralrs118203606
openSNPrs118203606
23andMers118203606
23andMe allrs118203606
SNP Nexus

SNPshotrs118203606
SNPdbers118203606
MSV3drs118203606
GWAS Ctlgrs118203606
Max Magnitude0
ClinVar
Risk rs118203606(T;T)
Alt rs118203606(T;T)
Reference rs118203606(C;C)
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.135781002G>A
CLNSRC Tuberous sclerosis database (TSC1)
CLNACC RCV000042110.2, RCV000189852.1,