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rs796053466

From SNPedia

Orientationminus
Make rs796053466(-;-)
Make rs796053466(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position132906137
GeneTSC1
is asnp
is mentioned by
dbSNPrs796053466
ebirs796053466
HLIrs796053466
Exacrs796053466
Varsomers796053466
Maprs796053466
PheGenIrs796053466
hapmaprs796053466
1000 genomesrs796053466
hgdprs796053466
ensemblrs796053466
gopubmedrs796053466
geneviewrs796053466
scholarrs796053466
googlers796053466
pharmgkbrs796053466
gwascentralrs796053466
openSNPrs796053466
23andMers796053466
23andMe allrs796053466
SNP Nexus

SNPshotrs796053466
SNPdbers796053466
MSV3drs796053466
GWAS Ctlgrs796053466
Max Magnitude
ClinVar
Risk rs796053466(;)
Alt rs796053466(;)
Reference rs796053466(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.135781524delC
CLNSRC
CLNACC RCV000189867.1,