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rs796053509

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053509(A;A)
Make rs796053509(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2079324
GeneTSC2
is asnp
is mentioned by
dbSNPrs796053509
ebirs796053509
HLIrs796053509
Exacrs796053509
Varsomers796053509
Maprs796053509
PheGenIrs796053509
hapmaprs796053509
1000 genomesrs796053509
hgdprs796053509
ensemblrs796053509
gopubmedrs796053509
geneviewrs796053509
scholarrs796053509
googlers796053509
pharmgkbrs796053509
gwascentralrs796053509
openSNPrs796053509
23andMers796053509
23andMe allrs796053509
SNP Nexus

SNPshotrs796053509
SNPdbers796053509
MSV3drs796053509
GWAS Ctlgrs796053509
Max Magnitude0
ClinVar
Risk rs796053509(A;A)
Alt rs796053509(A;A)
Reference rs796053509(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2129325G>A
CLNSRC
CLNACC RCV000190069.1,