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rs1085307762

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome16
Position2079403
GeneTSC2
is asnp
is mentioned by
dbSNPrs1085307762
dbSNP (old)rs1085307762
ClinGenrs1085307762
ebirs1085307762
HLIrs1085307762
Exacrs1085307762
Gnomadrs1085307762
Varsomers1085307762
Maprs1085307762
PheGenIrs1085307762
Biobankrs1085307762
1000 genomesrs1085307762
hgdprs1085307762
ensemblrs1085307762
gopubmedrs1085307762
geneviewrs1085307762
scholarrs1085307762
googlers1085307762
pharmgkbrs1085307762
gwascentralrs1085307762
openSNPrs1085307762
23andMers1085307762
23andMe allrs1085307762
SNPshotrs1085307762
SNPdbers1085307762
MSV3drs1085307762
GWAS Ctlgrs1085307762
Max Magnitude0
ClinVar
Risk rs1085307762(T;T)
Alt rs1085307762(T;T)
Reference Rs1085307762(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2129404G>T
CLNSRC
CLNACC RCV000490146.1,