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rs796053520

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGGTG;AGGTG) 0 common in clinvar
Make rs796053520(-;-)
Make rs796053520(-;TGAGG)
Make rs796053520(TGAGG;TGAGG)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position2085324
GeneTSC2
is asnp
is mentioned by
dbSNPrs796053520
ClinGenrs796053520
ebirs796053520
HLIrs796053520
Exacrs796053520
Varsomers796053520
Maprs796053520
PheGenIrs796053520
hapmaprs796053520
1000 genomesrs796053520
hgdprs796053520
ensemblrs796053520
gopubmedrs796053520
geneviewrs796053520
scholarrs796053520
googlers796053520
pharmgkbrs796053520
gwascentralrs796053520
openSNPrs796053520
23andMers796053520
23andMe allrs796053520
SNP Nexus

SNPshotrs796053520
SNPdbers796053520
MSV3drs796053520
GWAS Ctlgrs796053520
Max Magnitude0
ClinVar
Risk rs796053520(-;-)
Alt rs796053520(-;-)
Reference Rs796053520(AGGTG;AGGTG)
Significance Pathogenic
Disease not provided
Variation info
Gene TSC2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.2135325_2135329delTGAGG
CLNSRC
CLNACC RCV000190089.1,