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rs118203668

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs118203668(A;A)
Make rs118203668(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position132902713
GeneTSC1
is asnp
is mentioned by
dbSNPrs118203668
dbSNP (old)rs118203668
ClinGenrs118203668
ebirs118203668
HLIrs118203668
Exacrs118203668
Gnomadrs118203668
Varsomers118203668
Maprs118203668
PheGenIrs118203668
Biobankrs118203668
1000 genomesrs118203668
hgdprs118203668
ensemblrs118203668
gopubmedrs118203668
geneviewrs118203668
scholarrs118203668
googlers118203668
pharmgkbrs118203668
gwascentralrs118203668
openSNPrs118203668
23andMers118203668
23andMe allrs118203668
SNPshotrs118203668
SNPdbers118203668
MSV3drs118203668
GWAS Ctlgrs118203668
Max Magnitude0
ClinVar
Risk rs118203668(A;A) rs118203668(G;G)
Alt rs118203668(A;A) rs118203668(G;G)
Reference Rs118203668(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.135778100G>C; NC_000009.11:g.135778100G>T
CLNSRC Tuberous sclerosis database (TSC1)
CLNACC RCV000042181.2, RCV000042180.2, RCV000422886.1,