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rs1057518217

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518217(A;G)
Make rs1057518217(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position132904456
GeneTSC1
is asnp
is mentioned by
dbSNPrs1057518217
dbSNP (classic)rs1057518217
ClinGenrs1057518217
ebirs1057518217
HLIrs1057518217
Exacrs1057518217
Gnomadrs1057518217
Varsomers1057518217
LitVarrs1057518217
Maprs1057518217
PheGenIrs1057518217
Biobankrs1057518217
1000 genomesrs1057518217
hgdprs1057518217
ensemblrs1057518217
geneviewrs1057518217
scholarrs1057518217
googlers1057518217
pharmgkbrs1057518217
gwascentralrs1057518217
openSNPrs1057518217
23andMers1057518217
23andMe allrs1057518217
SNPshotrs1057518217
SNPdbers1057518217
MSV3drs1057518217
GWAS Ctlgrs1057518217
Max Magnitude0
ClinVar
Risk rs1057518217(G;G)
Alt rs1057518217(G;G)
Reference Rs1057518217(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.135779843T>C
CLNSRC
CLNACC RCV000413689.1,