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rs137853977

From SNPedia

Orientationplus
Make rs137853977(-;-)
Make rs137853977(-;AT)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2057156
GeneTSC2
is asnp
is mentioned by
dbSNPrs137853977
ebirs137853977
HLIrs137853977
Exacrs137853977
Varsomers137853977
Maprs137853977
PheGenIrs137853977
hapmaprs137853977
1000 genomesrs137853977
hgdprs137853977
ensemblrs137853977
gopubmedrs137853977
geneviewrs137853977
scholarrs137853977
googlers137853977
pharmgkbrs137853977
gwascentralrs137853977
openSNPrs137853977
23andMers137853977
23andMe allrs137853977
SNP Nexus

SNPshotrs137853977
SNPdbers137853977
MSV3drs137853977
GWAS Ctlgrs137853977
Max Magnitude
ClinVar
Risk rs137853977(;)
Alt rs137853977(;)
Reference rs137853977(AT;AT)
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.2107157_2107158delAT
CLNSRC Tuberous sclerosis database (TSC2)
CLNACC RCV000042707.2, RCV000180518.2,