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rs118203726

From SNPedia

Orientationminus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs118203726(-;-)
Make rs118203726(-;AG)
Make rs118203726(AG;AG)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position132897561
GeneTSC1
is asnp
is mentioned by
dbSNPrs118203726
ebirs118203726
HLIrs118203726
Exacrs118203726
Varsomers118203726
Maprs118203726
PheGenIrs118203726
hapmaprs118203726
1000 genomesrs118203726
hgdprs118203726
ensemblrs118203726
gopubmedrs118203726
geneviewrs118203726
scholarrs118203726
googlers118203726
pharmgkbrs118203726
gwascentralrs118203726
openSNPrs118203726
23andMers118203726
23andMe allrs118203726
SNP Nexus

SNPshotrs118203726
SNPdbers118203726
MSV3drs118203726
GWAS Ctlgrs118203726
Max Magnitude0
ClinVar
Risk rs118203726(;)
Alt rs118203726(;)
Reference rs118203726(GA;GA)
Significance Pathogenic
Disease Tuberous sclerosis syndrome Tuberous sclerosis 1
Variation info
Gene TSC1
CLNDBN Tuberous sclerosis syndrome Tuberous sclerosis 1
Reversed 1
HGVS NC_000009.11:g.135772947_135772948delTC
CLNSRC Tuberous sclerosis database (TSC1)
CLNACC RCV000042241.2, RCV000201049.1,