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rs878854115

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878854115(-;-)
Make rs878854115(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position2088119
GeneTSC2
is asnp
is mentioned by
dbSNPrs878854115
ebirs878854115
HLIrs878854115
Exacrs878854115
Varsomers878854115
Maprs878854115
PheGenIrs878854115
hapmaprs878854115
1000 genomesrs878854115
hgdprs878854115
ensemblrs878854115
gopubmedrs878854115
geneviewrs878854115
scholarrs878854115
googlers878854115
pharmgkbrs878854115
gwascentralrs878854115
openSNPrs878854115
23andMers878854115
23andMe allrs878854115
SNP Nexus

SNPshotrs878854115
SNPdbers878854115
MSV3drs878854115
GWAS Ctlgrs878854115
Max Magnitude0
ClinVar
Risk rs878854115(;)
Alt rs878854115(;)
Reference rs878854115(C;C)
Significance Probable-Pathogenic
Disease Tuberous sclerosis 2
Variation info
Gene TSC2
CLNDBN Tuberous sclerosis 2
Reversed 0
HGVS NC_000016.9:g.2138120delC
CLNSRC
CLNACC RCV000227937.1,