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rs1064796970

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome16
Position2086818
GeneTSC2
is asnp
is mentioned by
dbSNPrs1064796970
dbSNP (old)rs1064796970
ClinGenrs1064796970
ebirs1064796970
HLIrs1064796970
Exacrs1064796970
Gnomadrs1064796970
Varsomers1064796970
Maprs1064796970
PheGenIrs1064796970
Biobankrs1064796970
1000 genomesrs1064796970
hgdprs1064796970
ensemblrs1064796970
gopubmedrs1064796970
geneviewrs1064796970
scholarrs1064796970
googlers1064796970
pharmgkbrs1064796970
gwascentralrs1064796970
openSNPrs1064796970
23andMers1064796970
23andMe allrs1064796970
SNPshotrs1064796970
SNPdbers1064796970
MSV3drs1064796970
GWAS Ctlgrs1064796970
Max Magnitude0
ClinVar
Risk rs1064796970(A;A)
Alt rs1064796970(A;A)
Reference Rs1064796970(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2136819G>A
CLNSRC
CLNACC RCV000480140.1,