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rs118203661

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs118203661(C;T)
Make rs118203661(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position132902769
GeneTSC1
is asnp
is mentioned by
dbSNPrs118203661
dbSNP (old)rs118203661
ClinGenrs118203661
ebirs118203661
HLIrs118203661
Exacrs118203661
Gnomadrs118203661
Varsomers118203661
Maprs118203661
PheGenIrs118203661
Biobankrs118203661
1000 genomesrs118203661
hgdprs118203661
ensemblrs118203661
gopubmedrs118203661
geneviewrs118203661
scholarrs118203661
googlers118203661
pharmgkbrs118203661
gwascentralrs118203661
openSNPrs118203661
23andMers118203661
23andMe allrs118203661
SNPshotrs118203661
SNPdbers118203661
MSV3drs118203661
GWAS Ctlgrs118203661
Max Magnitude0
ClinVar
Risk rs118203661(T;T)
Alt rs118203661(T;T)
Reference Rs118203661(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.135778156G>A
CLNSRC Tuberous sclerosis database (TSC1)
CLNACC RCV000042172.2, RCV000414029.1,