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rs876658637

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658637(-;-)
Make rs876658637(-;CA)
Make rs876658637(CA;CA)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position224520
GeneSDHA
is asnp
is mentioned by
dbSNPrs876658637
ebirs876658637
HLIrs876658637
Exacrs876658637
Varsomers876658637
Maprs876658637
PheGenIrs876658637
hapmaprs876658637
1000 genomesrs876658637
hgdprs876658637
ensemblrs876658637
gopubmedrs876658637
geneviewrs876658637
scholarrs876658637
googlers876658637
pharmgkbrs876658637
gwascentralrs876658637
openSNPrs876658637
23andMers876658637
23andMe allrs876658637
SNP Nexus

SNPshotrs876658637
SNPdbers876658637
MSV3drs876658637
GWAS Ctlgrs876658637
Max Magnitude0
ClinVar
Risk rs876658637(CA;CA)
Alt rs876658637(CA;CA)
Reference rs876658637(;)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene SDHA
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000005.9:g.224634_224635dupCA
CLNSRC
CLNACC RCV000216352.1,