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rs876658367

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658367(A;A)
Make rs876658367(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position17024028
GeneSDHB
is asnp
is mentioned by
dbSNPrs876658367
ebirs876658367
HLIrs876658367
Exacrs876658367
Varsomers876658367
Maprs876658367
PheGenIrs876658367
hapmaprs876658367
1000 genomesrs876658367
hgdprs876658367
ensemblrs876658367
gopubmedrs876658367
geneviewrs876658367
scholarrs876658367
googlers876658367
pharmgkbrs876658367
gwascentralrs876658367
openSNPrs876658367
23andMers876658367
23andMe allrs876658367
SNP Nexus

SNPshotrs876658367
SNPdbers876658367
MSV3drs876658367
GWAS Ctlgrs876658367
Max Magnitude0
ClinVar
Risk rs876658367(A;A)
Alt rs876658367(A;A)
Reference rs876658367(G;G)
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.17350523C>T
CLNSRC
CLNACC RCV000220162.1,