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rs786205165

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205165(G;T)
Make rs786205165(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position11157173
GeneMTOR
is asnp
is mentioned by
dbSNPrs786205165
ebirs786205165
HLIrs786205165
Exacrs786205165
Varsomers786205165
Maprs786205165
PheGenIrs786205165
hapmaprs786205165
1000 genomesrs786205165
hgdprs786205165
ensemblrs786205165
gopubmedrs786205165
geneviewrs786205165
scholarrs786205165
googlers786205165
pharmgkbrs786205165
gwascentralrs786205165
openSNPrs786205165
23andMers786205165
23andMe allrs786205165
SNP Nexus

SNPshotrs786205165
SNPdbers786205165
MSV3drs786205165
GWAS Ctlgrs786205165
Max Magnitude0
ClinVar
Risk rs786205165(T;T)
Alt rs786205165(T;T)
Reference rs786205165(G;G)
Significance Pathogenic
Disease Smith-Kingsmore syndrome not provided
Variation info
Gene MTOR
CLNDBN Smith-Kingsmore syndrome not provided
Reversed 1
HGVS NC_000001.10:g.11217230C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000170355.4, RCV000224544.1,