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rs878854105

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878854105(-;-)
Make rs878854105(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position2084695
GeneTSC2
is asnp
is mentioned by
dbSNPrs878854105
ebirs878854105
HLIrs878854105
Exacrs878854105
Varsomers878854105
Maprs878854105
PheGenIrs878854105
hapmaprs878854105
1000 genomesrs878854105
hgdprs878854105
ensemblrs878854105
gopubmedrs878854105
geneviewrs878854105
scholarrs878854105
googlers878854105
pharmgkbrs878854105
gwascentralrs878854105
openSNPrs878854105
23andMers878854105
23andMe allrs878854105
SNP Nexus

SNPshotrs878854105
SNPdbers878854105
MSV3drs878854105
GWAS Ctlgrs878854105
Max Magnitude0
ClinVar
Risk rs878854105(;)
Alt rs878854105(;)
Reference rs878854105(A;A)
Significance Pathogenic
Disease Tuberous sclerosis 2
Variation info
Gene TSC2
CLNDBN Tuberous sclerosis 2
Reversed 0
HGVS NC_000016.9:g.2134696delA
CLNSRC
CLNACC RCV000233034.1,