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rs1064794132

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome9
Position132903649
GeneTSC1
is asnp
is mentioned by
dbSNPrs1064794132
dbSNP (old)rs1064794132
ClinGenrs1064794132
ebirs1064794132
HLIrs1064794132
Exacrs1064794132
Gnomadrs1064794132
Varsomers1064794132
Maprs1064794132
PheGenIrs1064794132
Biobankrs1064794132
1000 genomesrs1064794132
hgdprs1064794132
ensemblrs1064794132
gopubmedrs1064794132
geneviewrs1064794132
scholarrs1064794132
googlers1064794132
pharmgkbrs1064794132
gwascentralrs1064794132
openSNPrs1064794132
23andMers1064794132
23andMe allrs1064794132
SNPshotrs1064794132
SNPdbers1064794132
MSV3drs1064794132
GWAS Ctlgrs1064794132
Max Magnitude0
ClinVar
Risk rs1064794132(A;A)
Alt rs1064794132(A;A)
Reference Rs1064794132(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.135779036A>T
CLNSRC
CLNACC RCV000487211.1,