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

rs118203402

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs118203402(C;C)
Make rs118203402(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position132921913
GeneTSC1
is asnp
is mentioned by
dbSNPrs118203402
dbSNP (classic)rs118203402
ClinGenrs118203402
ebirs118203402
HLIrs118203402
Exacrs118203402
Gnomadrs118203402
Varsomers118203402
LitVarrs118203402
Maprs118203402
PheGenIrs118203402
Biobankrs118203402
1000 genomesrs118203402
hgdprs118203402
ensemblrs118203402
geneviewrs118203402
scholarrs118203402
googlers118203402
pharmgkbrs118203402
gwascentralrs118203402
openSNPrs118203402
23andMers118203402
23andMe allrs118203402
SNPshotrs118203402
SNPdbers118203402
MSV3drs118203402
GWAS Ctlgrs118203402
Max Magnitude0
ClinVar
Risk rs118203402(A;A) rs118203402(C;C)
Alt rs118203402(A;A) rs118203402(C;C)
Reference Rs118203402(G;G)
Significance Probable-Pathogenic
Disease Tuberous sclerosis syndrome not provided
Variation info
Gene TSC1
CLNDBN Tuberous sclerosis syndrome not provided
Reversed 1
HGVS NC_000009.11:g.135797300C>G
CLNSRC Tuberous sclerosis database (TSC1)
CLNACC RCV000042311.2, RCV000442086.1,