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rs1057520759

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520759(G;T)
Make rs1057520759(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position2081711
GeneTSC2
is asnp
is mentioned by
dbSNPrs1057520759
dbSNP (old)rs1057520759
ClinGenrs1057520759
ebirs1057520759
HLIrs1057520759
Exacrs1057520759
Gnomadrs1057520759
Varsomers1057520759
Maprs1057520759
PheGenIrs1057520759
Biobankrs1057520759
1000 genomesrs1057520759
hgdprs1057520759
ensemblrs1057520759
gopubmedrs1057520759
geneviewrs1057520759
scholarrs1057520759
googlers1057520759
pharmgkbrs1057520759
gwascentralrs1057520759
openSNPrs1057520759
23andMers1057520759
23andMe allrs1057520759
SNPshotrs1057520759
SNPdbers1057520759
MSV3drs1057520759
GWAS Ctlgrs1057520759
Max Magnitude0
ClinVar
Risk rs1057520759(T;T)
Alt rs1057520759(T;T)
Reference Rs1057520759(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2131712G>T
CLNSRC
CLNACC RCV000434569.1,