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rs876658461

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658461(C;T)
Make rs876658461(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position17023975
GeneSDHB
is asnp
is mentioned by
dbSNPrs876658461
ebirs876658461
HLIrs876658461
Exacrs876658461
Varsomers876658461
Maprs876658461
PheGenIrs876658461
hapmaprs876658461
1000 genomesrs876658461
hgdprs876658461
ensemblrs876658461
gopubmedrs876658461
geneviewrs876658461
scholarrs876658461
googlers876658461
pharmgkbrs876658461
gwascentralrs876658461
openSNPrs876658461
23andMers876658461
23andMe allrs876658461
SNP Nexus

SNPshotrs876658461
SNPdbers876658461
MSV3drs876658461
GWAS Ctlgrs876658461
Max Magnitude0
ClinVar
Risk rs876658461(T;T)
Alt rs876658461(T;T)
Reference rs876658461(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Paragangliomas 4
Variation info
Gene SDHB
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Paragangliomas 4
Reversed 1
HGVS NC_000001.10:g.17350470G>A
CLNSRC
CLNACC RCV000215175.1, RCV000238597.1,