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rs794727906

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727906(C;C)
Make rs794727906(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2056643
GeneTSC2
is asnp
is mentioned by
dbSNPrs794727906
ebirs794727906
HLIrs794727906
Exacrs794727906
Varsomers794727906
Maprs794727906
PheGenIrs794727906
hapmaprs794727906
1000 genomesrs794727906
hgdprs794727906
ensemblrs794727906
gopubmedrs794727906
geneviewrs794727906
scholarrs794727906
googlers794727906
pharmgkbrs794727906
gwascentralrs794727906
openSNPrs794727906
23andMers794727906
23andMe allrs794727906
SNP Nexus

SNPshotrs794727906
SNPdbers794727906
MSV3drs794727906
GWAS Ctlgrs794727906
Max Magnitude0
ClinVar
Risk rs794727906(C;C)
Alt rs794727906(C;C)
Reference rs794727906(G;G)
Significance Pathogenic
Disease Tuberous sclerosis 2
Variation info
Gene TSC2
CLNDBN Tuberous sclerosis 2
Reversed 0
HGVS NC_000016.9:g.2106644G>C
CLNSRC
CLNACC RCV000180176.1,