Have questions? Visit https://www.reddit.com/r/SNPedia

rs869312666

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869312666(G;G)
Make rs869312666(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position11129789
GeneMTOR
is asnp
is mentioned by
dbSNPrs869312666
ebirs869312666
HLIrs869312666
Exacrs869312666
Varsomers869312666
Maprs869312666
PheGenIrs869312666
hapmaprs869312666
1000 genomesrs869312666
hgdprs869312666
ensemblrs869312666
gopubmedrs869312666
geneviewrs869312666
scholarrs869312666
googlers869312666
pharmgkbrs869312666
gwascentralrs869312666
openSNPrs869312666
23andMers869312666
23andMe allrs869312666
SNP Nexus

SNPshotrs869312666
SNPdbers869312666
MSV3drs869312666
GWAS Ctlgrs869312666
Max Magnitude0
ClinVar
Risk rs869312666(G;G)
Alt rs869312666(G;G)
Reference rs869312666(T;T)
Significance Pathogenic
Disease Smith-Kingsmore syndrome
Variation info
Gene MTOR
CLNDBN Smith-Kingsmore syndrome
Reversed 1
HGVS NC_000001.10:g.11189846A>C
CLNSRC
CLNACC RCV000209915.1,