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rs397515226

From SNPedia

Orientationplus
Make rs397515226(-;-)
Make rs397515226(-;AG)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2071796
GeneTSC2
is asnp
is mentioned by
dbSNPrs397515226
ebirs397515226
HLIrs397515226
Exacrs397515226
Varsomers397515226
Maprs397515226
PheGenIrs397515226
hapmaprs397515226
1000 genomesrs397515226
hgdprs397515226
ensemblrs397515226
gopubmedrs397515226
geneviewrs397515226
scholarrs397515226
googlers397515226
pharmgkbrs397515226
gwascentralrs397515226
openSNPrs397515226
23andMers397515226
23andMe allrs397515226
SNP Nexus

SNPshotrs397515226
SNPdbers397515226
MSV3drs397515226
GWAS Ctlgrs397515226
Max Magnitude
ClinVar
Risk rs397515226(;)
Alt rs397515226(;)
Reference rs397515226(AG;AG)
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.2121797_2121798delAG
CLNSRC Tuberous sclerosis database (TSC2)
CLNACC RCV000055533.1, RCV000201097.1,