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rs876659491

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659491(-;-)
Make rs876659491(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position17027847
GeneSDHB
is asnp
is mentioned by
dbSNPrs876659491
ebirs876659491
HLIrs876659491
Exacrs876659491
Varsomers876659491
Maprs876659491
PheGenIrs876659491
hapmaprs876659491
1000 genomesrs876659491
hgdprs876659491
ensemblrs876659491
gopubmedrs876659491
geneviewrs876659491
scholarrs876659491
googlers876659491
pharmgkbrs876659491
gwascentralrs876659491
openSNPrs876659491
23andMers876659491
23andMe allrs876659491
SNP Nexus

SNPshotrs876659491
SNPdbers876659491
MSV3drs876659491
GWAS Ctlgrs876659491
Max Magnitude0
ClinVar
Risk rs876659491(;)
Alt rs876659491(;)
Reference rs876659491(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.17354342delC
CLNSRC
CLNACC RCV000220488.1,