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rs137853977

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;AT) 6.3 Tuberous Sclerosis Complex
(AT;AT) 0 common in clinvar


Make rs137853977(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2057156
GeneTSC2
is asnp
is mentioned by
dbSNPrs137853977
dbSNP (classic)rs137853977
ClinGenrs137853977
ebirs137853977
HLIrs137853977
Exacrs137853977
Gnomadrs137853977
Varsomers137853977
LitVarrs137853977
Maprs137853977
PheGenIrs137853977
Biobankrs137853977
1000 genomesrs137853977
hgdprs137853977
ensemblrs137853977
geneviewrs137853977
scholarrs137853977
googlers137853977
pharmgkbrs137853977
gwascentralrs137853977
openSNPrs137853977
23andMers137853977
SNPshotrs137853977
SNPdbers137853977
MSV3drs137853977
GWAS Ctlgrs137853977
Max Magnitude6.3
ClinVar
Risk rs137853977(-;-)
Alt rs137853977(-;-)
Reference Rs137853977(AT;AT)
Significance Pathogenic
Disease Tuberous sclerosis syndrome Tuberous sclerosis 2 not provided
Variation info
Gene TSC2
CLNDBN Tuberous sclerosis syndrome Tuberous sclerosis 2 not provided
Reversed 0
HGVS NC_000016.9:g.2107157_2107158delAT
CLNSRC Tuberous sclerosis database (TSC2)
CLNACC RCV000042707.2, RCV000180518.2, RCV000312270.1,