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rs876658350

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658350(A;A)
Make rs876658350(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position61438090
GeneSDHAF2
is asnp
is mentioned by
dbSNPrs876658350
ebirs876658350
HLIrs876658350
Exacrs876658350
Varsomers876658350
Maprs876658350
PheGenIrs876658350
hapmaprs876658350
1000 genomesrs876658350
hgdprs876658350
ensemblrs876658350
gopubmedrs876658350
geneviewrs876658350
scholarrs876658350
googlers876658350
pharmgkbrs876658350
gwascentralrs876658350
openSNPrs876658350
23andMers876658350
23andMe allrs876658350
SNP Nexus

SNPshotrs876658350
SNPdbers876658350
MSV3drs876658350
GWAS Ctlgrs876658350
Max Magnitude0
ClinVar
Risk rs876658350(A;A)
Alt rs876658350(A;A)
Reference rs876658350(G;G)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene SDHAF2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.61205562G>A
CLNSRC
CLNACC RCV000213784.1,