Have questions? Visit https://www.reddit.com/r/SNPedia

rs1085307853

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome16
Position2084227
GeneTSC2
is asnp
is mentioned by
dbSNPrs1085307853
dbSNP (classic)rs1085307853
ClinGenrs1085307853
ebirs1085307853
HLIrs1085307853
Exacrs1085307853
Gnomadrs1085307853
Varsomers1085307853
LitVarrs1085307853
Maprs1085307853
PheGenIrs1085307853
Biobankrs1085307853
1000 genomesrs1085307853
hgdprs1085307853
ensemblrs1085307853
geneviewrs1085307853
scholarrs1085307853
googlers1085307853
pharmgkbrs1085307853
gwascentralrs1085307853
openSNPrs1085307853
23andMers1085307853
23andMe allrs1085307853
SNPshotrs1085307853
SNPdbers1085307853
MSV3drs1085307853
GWAS Ctlgrs1085307853
Max Magnitude0
ClinVar
Risk rs1085307853(A;A)
Alt rs1085307853(A;A)
Reference Rs1085307853(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2134228G>A
CLNSRC
CLNACC RCV000490195.1,