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rs876658540

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658540(G;T)
Make rs876658540(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position17024049
GeneSDHB
is asnp
is mentioned by
dbSNPrs876658540
ebirs876658540
HLIrs876658540
Exacrs876658540
Varsomers876658540
Maprs876658540
PheGenIrs876658540
hapmaprs876658540
1000 genomesrs876658540
hgdprs876658540
ensemblrs876658540
gopubmedrs876658540
geneviewrs876658540
scholarrs876658540
googlers876658540
pharmgkbrs876658540
gwascentralrs876658540
openSNPrs876658540
23andMers876658540
23andMe allrs876658540
SNP Nexus

SNPshotrs876658540
SNPdbers876658540
MSV3drs876658540
GWAS Ctlgrs876658540
Max Magnitude0
ClinVar
Risk rs876658540(T;T)
Alt rs876658540(T;T)
Reference rs876658540(G;G)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene SDHB
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000001.10:g.17350544C>A
CLNSRC
CLNACC RCV000215934.1,