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rs45469298

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs45469298(C;G)
Make rs45469298(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2070570
GeneTSC2
is asnp
is mentioned by
dbSNPrs45469298
ebirs45469298
HLIrs45469298
Exacrs45469298
Varsomers45469298
Maprs45469298
PheGenIrs45469298
hapmaprs45469298
1000 genomesrs45469298
hgdprs45469298
ensemblrs45469298
gopubmedrs45469298
geneviewrs45469298
scholarrs45469298
googlers45469298
pharmgkbrs45469298
gwascentralrs45469298
openSNPrs45469298
23andMers45469298
23andMe allrs45469298
SNP Nexus

SNPshotrs45469298
SNPdbers45469298
MSV3drs45469298
GWAS Ctlgrs45469298
Max Magnitude0
ClinVar
Risk rs45469298(G,T;G,T)
Alt rs45469298(G,T;G,T)
Reference rs45469298(C;C)
Significance Pathogenic
Disease Tuberous sclerosis syndrome not provided
Variation info
Gene TSC2
CLNDBN Tuberous sclerosis syndrome not provided
Reversed 0
HGVS NC_000016.9:g.2120571C>G; NC_000016.9:g.2120571C>T
CLNSRC Tuberous sclerosis database (TSC2)
CLNACC RCV000042433.2, RCV000042905.2, RCV000189989.1,