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rs796053464

From SNPedia

Orientationminus
Make rs796053464(-;-)
Make rs796053464(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position132921895
GeneTSC1
is asnp
is mentioned by
dbSNPrs796053464
ebirs796053464
HLIrs796053464
Exacrs796053464
Varsomers796053464
Maprs796053464
PheGenIrs796053464
hapmaprs796053464
1000 genomesrs796053464
hgdprs796053464
ensemblrs796053464
gopubmedrs796053464
geneviewrs796053464
scholarrs796053464
googlers796053464
pharmgkbrs796053464
gwascentralrs796053464
openSNPrs796053464
23andMers796053464
23andMe allrs796053464
SNP Nexus

SNPshotrs796053464
SNPdbers796053464
MSV3drs796053464
GWAS Ctlgrs796053464
Max Magnitude
ClinVar
Risk rs796053464(;)
Alt rs796053464(;)
Reference rs796053464(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC1
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.135797282delG
CLNSRC
CLNACC RCV000189864.1,