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rs587777900

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777900(A;A)
Make rs587777900(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position11114363
GeneMTOR
is asnp
is mentioned by
dbSNPrs587777900
dbSNP (classic)rs587777900
ClinGenrs587777900
ebirs587777900
HLIrs587777900
Exacrs587777900
Gnomadrs587777900
Varsomers587777900
LitVarrs587777900
Maprs587777900
PheGenIrs587777900
Biobankrs587777900
1000 genomesrs587777900
hgdprs587777900
ensemblrs587777900
geneviewrs587777900
scholarrs587777900
googlers587777900
pharmgkbrs587777900
gwascentralrs587777900
openSNPrs587777900
23andMers587777900
SNPshotrs587777900
SNPdbers587777900
MSV3drs587777900
GWAS Ctlgrs587777900
Max Magnitude0
ClinVar
Risk rs587777900(A;A)
Alt rs587777900(A;A)
Reference Rs587777900(G;G)
Significance Probable-Pathogenic
Disease not provided Transitional cell carcinoma of the bladder
Variation info
Gene MTOR
CLNDBN not provided Transitional cell carcinoma of the bladder
Reversed 1
HGVS NC_000001.10:g.11174420C>T
CLNSRC
CLNACC RCV000190287.1, RCV000429790.1,