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rs1057518508

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518508(-;-)
Make rs1057518508(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position2054387
GeneTSC2
is asnp
is mentioned by
dbSNPrs1057518508
dbSNP (old)rs1057518508
ClinGenrs1057518508
ebirs1057518508
HLIrs1057518508
Exacrs1057518508
Gnomadrs1057518508
Varsomers1057518508
Maprs1057518508
PheGenIrs1057518508
Biobankrs1057518508
1000 genomesrs1057518508
hgdprs1057518508
ensemblrs1057518508
gopubmedrs1057518508
geneviewrs1057518508
scholarrs1057518508
googlers1057518508
pharmgkbrs1057518508
gwascentralrs1057518508
openSNPrs1057518508
23andMers1057518508
23andMe allrs1057518508
SNPshotrs1057518508
SNPdbers1057518508
MSV3drs1057518508
GWAS Ctlgrs1057518508
Max Magnitude0
ClinVar
Risk rs1057518508(-;-)
Alt rs1057518508(-;-)
Reference Rs1057518508(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2104388delT
CLNSRC
CLNACC RCV000413504.1,