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rs878854075

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs878854075(-;T)
Make rs878854075(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position2061911
GeneTSC2
is asnp
is mentioned by
dbSNPrs878854075
dbSNP (classic)rs878854075
ClinGenrs878854075
ebirs878854075
HLIrs878854075
Exacrs878854075
Gnomadrs878854075
Varsomers878854075
LitVarrs878854075
Maprs878854075
PheGenIrs878854075
Biobankrs878854075
1000 genomesrs878854075
hgdprs878854075
ensemblrs878854075
geneviewrs878854075
scholarrs878854075
googlers878854075
pharmgkbrs878854075
gwascentralrs878854075
openSNPrs878854075
23andMers878854075
SNPshotrs878854075
SNPdbers878854075
MSV3drs878854075
GWAS Ctlgrs878854075
Max Magnitude0
ClinVar
Risk rs878854075(T;T)
Alt rs878854075(T;T)
Reference Rs878854075(-;-)
Significance Pathogenic
Disease Tuberous sclerosis 2
Variation info
Gene TSC2
CLNDBN Tuberous sclerosis 2
Reversed 0
HGVS NC_000016.9:g.2111912dupT
CLNSRC
CLNACC RCV000228535.1,