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rs1057523727

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057523727(C;C)
Make rs1057523727(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position2060813
GeneTSC2
is asnp
is mentioned by
dbSNPrs1057523727
dbSNP (old)rs1057523727
ClinGenrs1057523727
ebirs1057523727
HLIrs1057523727
Exacrs1057523727
Gnomadrs1057523727
Varsomers1057523727
Maprs1057523727
PheGenIrs1057523727
Biobankrs1057523727
1000 genomesrs1057523727
hgdprs1057523727
ensemblrs1057523727
gopubmedrs1057523727
geneviewrs1057523727
scholarrs1057523727
googlers1057523727
pharmgkbrs1057523727
gwascentralrs1057523727
openSNPrs1057523727
23andMers1057523727
23andMe allrs1057523727
SNPshotrs1057523727
SNPdbers1057523727
MSV3drs1057523727
GWAS Ctlgrs1057523727
Max Magnitude0
ClinVar
Risk rs1057523727(C;C)
Alt rs1057523727(C;C)
Reference Rs1057523727(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2110814G>C
CLNSRC
CLNACC RCV000445030.1,