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rs1064793797

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome16
Position2083763
GeneTSC2
is asnp
is mentioned by
dbSNPrs1064793797
dbSNP (classic)rs1064793797
ClinGenrs1064793797
ebirs1064793797
HLIrs1064793797
Exacrs1064793797
Gnomadrs1064793797
Varsomers1064793797
LitVarrs1064793797
Maprs1064793797
PheGenIrs1064793797
Biobankrs1064793797
1000 genomesrs1064793797
hgdprs1064793797
ensemblrs1064793797
geneviewrs1064793797
scholarrs1064793797
googlers1064793797
pharmgkbrs1064793797
gwascentralrs1064793797
openSNPrs1064793797
23andMers1064793797
23andMe allrs1064793797
SNPshotrs1064793797
SNPdbers1064793797
MSV3drs1064793797
GWAS Ctlgrs1064793797
Max Magnitude0
ClinVar
Risk rs1064793797(T;T)
Alt rs1064793797(T;T)
Reference Rs1064793797(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2133764G>T
CLNSRC
CLNACC RCV000483948.1,