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rs876658451

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658451(C;T)
Make rs876658451(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position17027844
GeneSDHB
is asnp
is mentioned by
dbSNPrs876658451
ebirs876658451
HLIrs876658451
Exacrs876658451
Varsomers876658451
Maprs876658451
PheGenIrs876658451
hapmaprs876658451
1000 genomesrs876658451
hgdprs876658451
ensemblrs876658451
gopubmedrs876658451
geneviewrs876658451
scholarrs876658451
googlers876658451
pharmgkbrs876658451
gwascentralrs876658451
openSNPrs876658451
23andMers876658451
23andMe allrs876658451
SNP Nexus

SNPshotrs876658451
SNPdbers876658451
MSV3drs876658451
GWAS Ctlgrs876658451
Max Magnitude0
ClinVar
Risk rs876658451(T;T)
Alt rs876658451(T;T)
Reference rs876658451(C;C)
Significance 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.17354339G>A
CLNSRC
CLNACC RCV000219011.1,