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rs1064793464

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome16
Position2080171
GeneTSC2
is asnp
is mentioned by
dbSNPrs1064793464
dbSNP (classic)rs1064793464
ClinGenrs1064793464
ebirs1064793464
HLIrs1064793464
Exacrs1064793464
Gnomadrs1064793464
Varsomers1064793464
LitVarrs1064793464
Maprs1064793464
PheGenIrs1064793464
Biobankrs1064793464
1000 genomesrs1064793464
hgdprs1064793464
ensemblrs1064793464
geneviewrs1064793464
scholarrs1064793464
googlers1064793464
pharmgkbrs1064793464
gwascentralrs1064793464
openSNPrs1064793464
23andMers1064793464
23andMe allrs1064793464
SNPshotrs1064793464
SNPdbers1064793464
MSV3drs1064793464
GWAS Ctlgrs1064793464
Max Magnitude0
ClinVar
Risk rs1064793464(-;-)
Alt rs1064793464(-;-)
Reference Rs1064793464(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2130172delA
CLNSRC
CLNACC RCV000478220.1,