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rs796053518

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGTCCAGCTGCCA;AGTCCAGCTGCCA) 0 common in clinvar
Make rs796053518(-;-)
Make rs796053518(-;TCCAGCTGCCAAG)
Make rs796053518(TCCAGCTGCCAAG;TCCAGCTGCCAAG)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2082462
GeneTSC2
is asnp
is mentioned by
dbSNPrs796053518
dbSNP (old)rs796053518
ClinGenrs796053518
ebirs796053518
HLIrs796053518
Exacrs796053518
Gnomadrs796053518
Varsomers796053518
Maprs796053518
PheGenIrs796053518
Biobankrs796053518
1000 genomesrs796053518
hgdprs796053518
ensemblrs796053518
gopubmedrs796053518
geneviewrs796053518
scholarrs796053518
googlers796053518
pharmgkbrs796053518
gwascentralrs796053518
openSNPrs796053518
23andMers796053518
23andMe allrs796053518
SNP Nexus

SNPshotrs796053518
SNPdbers796053518
MSV3drs796053518
GWAS Ctlgrs796053518
Max Magnitude0
ClinVar
Risk rs796053518(-;-)
Alt rs796053518(-;-)
Reference Rs796053518(AGTCCAGCTGCCA;AGTCCAGCTGCCA)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2132463_2132475delTCCAGCTGCCAAG
CLNSRC
CLNACC RCV000190087.1,