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rs1057522911

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057522911(C;C)
Make rs1057522911(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position2074372
GeneTSC2
is asnp
is mentioned by
dbSNPrs1057522911
dbSNP (old)rs1057522911
ClinGenrs1057522911
ebirs1057522911
HLIrs1057522911
Exacrs1057522911
Gnomadrs1057522911
Varsomers1057522911
LitVarrs1057522911
Maprs1057522911
PheGenIrs1057522911
Biobankrs1057522911
1000 genomesrs1057522911
hgdprs1057522911
ensemblrs1057522911
gopubmedrs1057522911
geneviewrs1057522911
scholarrs1057522911
googlers1057522911
pharmgkbrs1057522911
gwascentralrs1057522911
openSNPrs1057522911
23andMers1057522911
23andMe allrs1057522911
SNPshotrs1057522911
SNPdbers1057522911
MSV3drs1057522911
GWAS Ctlgrs1057522911
Max Magnitude0
ClinVar
Risk rs1057522911(C;C)
Alt rs1057522911(C;C)
Reference Rs1057522911(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2124373T>C
CLNSRC
CLNACC RCV000433607.1,