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rs794728947

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794728947(-;-)
Make rs794728947(-;C)
Make rs794728947(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position17033135
GeneSDHB
is asnp
is mentioned by
dbSNPrs794728947
ebirs794728947
HLIrs794728947
Exacrs794728947
Varsomers794728947
Maprs794728947
PheGenIrs794728947
hapmaprs794728947
1000 genomesrs794728947
hgdprs794728947
ensemblrs794728947
gopubmedrs794728947
geneviewrs794728947
scholarrs794728947
googlers794728947
pharmgkbrs794728947
gwascentralrs794728947
openSNPrs794728947
23andMers794728947
23andMe allrs794728947
SNP Nexus

SNPshotrs794728947
SNPdbers794728947
MSV3drs794728947
GWAS Ctlgrs794728947
Max Magnitude0
ClinVar
Risk rs794728947(C;C)
Alt rs794728947(C;C)
Reference rs794728947(;)
Significance Pathogenic
Disease not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene SDHB
CLNDBN not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000001.10:g.17359631dupG
CLNSRC
CLNACC RCV000183218.1, RCV000216710.1,