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rs137854210

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs137854210(-;T)
Make rs137854210(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2081680
GeneTSC2
is asnp
is mentioned by
dbSNPrs137854210
dbSNP (old)rs137854210
ClinGenrs137854210
ebirs137854210
HLIrs137854210
Exacrs137854210
Gnomadrs137854210
Varsomers137854210
Maprs137854210
PheGenIrs137854210
Biobankrs137854210
1000 genomesrs137854210
hgdprs137854210
ensemblrs137854210
gopubmedrs137854210
geneviewrs137854210
scholarrs137854210
googlers137854210
pharmgkbrs137854210
gwascentralrs137854210
openSNPrs137854210
23andMers137854210
23andMe allrs137854210
SNP Nexus

SNPshotrs137854210
SNPdbers137854210
MSV3drs137854210
GWAS Ctlgrs137854210
Max Magnitude0
ClinVar
Risk rs137854210(T;T)
Alt rs137854210(T;T)
Reference Rs137854210(-;-)
Significance Pathogenic
Disease Tuberous sclerosis syndrome Tuberous sclerosis 2
Variation info
Gene TSC2
CLNDBN Tuberous sclerosis syndrome Tuberous sclerosis 2
Reversed 0
HGVS NC_000016.9:g.2131681dupT
CLNSRC Tuberous sclerosis database (TSC2)
CLNACC RCV000042799.2, RCV000201083.1,