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rs1064796511

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome16
Position2053444
GeneTSC2
is asnp
is mentioned by
dbSNPrs1064796511
dbSNP (old)rs1064796511
ClinGenrs1064796511
ebirs1064796511
HLIrs1064796511
Exacrs1064796511
Gnomadrs1064796511
Varsomers1064796511
Maprs1064796511
PheGenIrs1064796511
Biobankrs1064796511
1000 genomesrs1064796511
hgdprs1064796511
ensemblrs1064796511
gopubmedrs1064796511
geneviewrs1064796511
scholarrs1064796511
googlers1064796511
pharmgkbrs1064796511
gwascentralrs1064796511
openSNPrs1064796511
23andMers1064796511
23andMe allrs1064796511
SNPshotrs1064796511
SNPdbers1064796511
MSV3drs1064796511
GWAS Ctlgrs1064796511
Max Magnitude0
ClinVar
Risk rs1064796511(T;T)
Alt rs1064796511(T;T)
Reference Rs1064796511(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2103445C>T
CLNSRC
CLNACC RCV000478118.1,