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rs118203610

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs118203610(A;A)
Make rs118203610(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position132905580
GeneTSC1
is asnp
is mentioned by
dbSNPrs118203610
ebirs118203610
HLIrs118203610
Exacrs118203610
Varsomers118203610
Maprs118203610
PheGenIrs118203610
hapmaprs118203610
1000 genomesrs118203610
hgdprs118203610
ensemblrs118203610
gopubmedrs118203610
geneviewrs118203610
scholarrs118203610
googlers118203610
pharmgkbrs118203610
gwascentralrs118203610
openSNPrs118203610
23andMers118203610
23andMe allrs118203610
SNP Nexus

SNPshotrs118203610
SNPdbers118203610
MSV3drs118203610
GWAS Ctlgrs118203610
Max Magnitude0
ClinVar
Risk rs118203610(A,C;A,C)
Alt rs118203610(A,C;A,C)
Reference rs118203610(G;G)
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.135780967C>G; NC_000009.11:g.135780967C>T
CLNSRC Tuberous sclerosis database (TSC1)
CLNACC RCV000042115.2, RCV000042114.2, RCV000189849.1,