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rs137854028

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854028(-;-)
Make rs137854028(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position2084994
GeneTSC2
is asnp
is mentioned by
dbSNPrs137854028
dbSNP (old)rs137854028
ClinGenrs137854028
ebirs137854028
HLIrs137854028
Exacrs137854028
Gnomadrs137854028
Varsomers137854028
LitVarrs137854028
Maprs137854028
PheGenIrs137854028
Biobankrs137854028
1000 genomesrs137854028
hgdprs137854028
ensemblrs137854028
gopubmedrs137854028
geneviewrs137854028
scholarrs137854028
googlers137854028
pharmgkbrs137854028
gwascentralrs137854028
openSNPrs137854028
23andMers137854028
23andMe allrs137854028
SNPshotrs137854028
SNPdbers137854028
MSV3drs137854028
GWAS Ctlgrs137854028
Max Magnitude0
ClinVar
Risk rs137854028(-;-)
Alt rs137854028(-;-)
Reference Rs137854028(G;G)
Significance Pathogenic
Disease Tuberous sclerosis syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene TSC2
CLNDBN Tuberous sclerosis syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000016.9:g.2134995delG
CLNSRC Tuberous sclerosis database (TSC2)
CLNACC RCV000042765.2, RCV000491824.1,