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rs876659330

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659330(C;C)
Make rs876659330(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position17044758
GeneSDHB
is asnp
is mentioned by
dbSNPrs876659330
ebirs876659330
HLIrs876659330
Exacrs876659330
Varsomers876659330
Maprs876659330
PheGenIrs876659330
hapmaprs876659330
1000 genomesrs876659330
hgdprs876659330
ensemblrs876659330
gopubmedrs876659330
geneviewrs876659330
scholarrs876659330
googlers876659330
pharmgkbrs876659330
gwascentralrs876659330
openSNPrs876659330
23andMers876659330
23andMe allrs876659330
SNP Nexus

SNPshotrs876659330
SNPdbers876659330
MSV3drs876659330
GWAS Ctlgrs876659330
Max Magnitude0
ClinVar
Risk rs876659330(C;C)
Alt rs876659330(C;C)
Reference rs876659330(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.17371253C>G
CLNSRC
CLNACC RCV000221442.1,