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rs1064793646

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome16
Position2086763
GeneTSC2
is asnp
is mentioned by
dbSNPrs1064793646
dbSNP (old)rs1064793646
ClinGenrs1064793646
ebirs1064793646
HLIrs1064793646
Exacrs1064793646
Gnomadrs1064793646
Varsomers1064793646
LitVarrs1064793646
Maprs1064793646
PheGenIrs1064793646
Biobankrs1064793646
1000 genomesrs1064793646
hgdprs1064793646
ensemblrs1064793646
gopubmedrs1064793646
geneviewrs1064793646
scholarrs1064793646
googlers1064793646
pharmgkbrs1064793646
gwascentralrs1064793646
openSNPrs1064793646
23andMers1064793646
23andMe allrs1064793646
SNPshotrs1064793646
SNPdbers1064793646
MSV3drs1064793646
GWAS Ctlgrs1064793646
Max Magnitude0
ClinVar
Risk rs1064793646(-;-)
Alt rs1064793646(-;-)
Reference Rs1064793646(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2136764delC
CLNSRC
CLNACC RCV000479318.1,