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rs137854036

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs137854036(-;-)
Make rs137854036(-;TG)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position2088139
GeneTSC2
is asnp
is mentioned by
dbSNPrs137854036
dbSNP (classic)rs137854036
ClinGenrs137854036
ebirs137854036
HLIrs137854036
Exacrs137854036
Gnomadrs137854036
Varsomers137854036
LitVarrs137854036
Maprs137854036
PheGenIrs137854036
Biobankrs137854036
1000 genomesrs137854036
hgdprs137854036
ensemblrs137854036
geneviewrs137854036
scholarrs137854036
googlers137854036
pharmgkbrs137854036
gwascentralrs137854036
openSNPrs137854036
23andMers137854036
23andMe allrs137854036
SNPshotrs137854036
SNPdbers137854036
MSV3drs137854036
GWAS Ctlgrs137854036
Max Magnitude0
ClinVar
Risk rs137854036(-;-)
Alt rs137854036(-;-)
Reference Rs137854036(TG;TG)
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.2138142_2138143delTG
CLNSRC Tuberous sclerosis database (TSC2)
CLNACC RCV000043252.2, RCV000489070.1,