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rs876658878

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs876658878(-;-)
Make rs876658878(-;AG)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position2054319
GeneTSC2
is asnp
is mentioned by
dbSNPrs876658878
ebirs876658878
HLIrs876658878
Exacrs876658878
Varsomers876658878
Maprs876658878
PheGenIrs876658878
hapmaprs876658878
1000 genomesrs876658878
hgdprs876658878
ensemblrs876658878
gopubmedrs876658878
geneviewrs876658878
scholarrs876658878
googlers876658878
pharmgkbrs876658878
gwascentralrs876658878
openSNPrs876658878
23andMers876658878
23andMe allrs876658878
SNP Nexus

SNPshotrs876658878
SNPdbers876658878
MSV3drs876658878
GWAS Ctlgrs876658878
Max Magnitude0
ClinVar
Risk rs876658878(;)
Alt rs876658878(;)
Reference rs876658878(AG;AG)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene TSC2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000016.9:g.2104320_2104321delAG
CLNSRC
CLNACC RCV000219250.1,