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rs876659595

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659595(A;A)
Make rs876659595(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position251469
GeneSDHA
is asnp
is mentioned by
dbSNPrs876659595
ebirs876659595
HLIrs876659595
Exacrs876659595
Varsomers876659595
Maprs876659595
PheGenIrs876659595
hapmaprs876659595
1000 genomesrs876659595
hgdprs876659595
ensemblrs876659595
gopubmedrs876659595
geneviewrs876659595
scholarrs876659595
googlers876659595
pharmgkbrs876659595
gwascentralrs876659595
openSNPrs876659595
23andMers876659595
23andMe allrs876659595
SNP Nexus

SNPshotrs876659595
SNPdbers876659595
MSV3drs876659595
GWAS Ctlgrs876659595
Max Magnitude0
ClinVar
Risk rs876659595(A;A)
Alt rs876659595(A;A)
Reference rs876659595(G;G)
Significance Probable-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.251584G>A
CLNSRC
CLNACC RCV000215067.1,