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rs118203564

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs118203564(-;-)
Make rs118203564(-;AG)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position132905869
GeneTSC1
is asnp
is mentioned by
dbSNPrs118203564
dbSNP (old)rs118203564
ClinGenrs118203564
ebirs118203564
HLIrs118203564
Exacrs118203564
Gnomadrs118203564
Varsomers118203564
Maprs118203564
PheGenIrs118203564
Biobankrs118203564
1000 genomesrs118203564
hgdprs118203564
ensemblrs118203564
gopubmedrs118203564
geneviewrs118203564
scholarrs118203564
googlers118203564
pharmgkbrs118203564
gwascentralrs118203564
openSNPrs118203564
23andMers118203564
23andMe allrs118203564
SNPshotrs118203564
SNPdbers118203564
MSV3drs118203564
GWAS Ctlgrs118203564
Max Magnitude0
ClinVar
Risk rs118203564(-;-)
Alt rs118203564(-;-)
Reference Rs118203564(AG;AG)
Significance Pathogenic
Disease Tuberous sclerosis syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene TSC1
CLNDBN Tuberous sclerosis syndrome Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000009.11:g.135781256_135781257delCT
CLNSRC Tuberous sclerosis database (TSC1)
CLNACC RCV000042066.2, RCV000491128.1,