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rs878854632

From SNPedia

Orientationplus
Geno Mag Summary
(CAG;CAG) 0 common in clinvar
Make rs878854632(-;-)
Make rs878854632(-;AGC)
Make rs878854632(AGC;AGC)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position225881
GeneSDHA
is asnp
is mentioned by
dbSNPrs878854632
ebirs878854632
HLIrs878854632
Exacrs878854632
Varsomers878854632
Maprs878854632
PheGenIrs878854632
hapmaprs878854632
1000 genomesrs878854632
hgdprs878854632
ensemblrs878854632
gopubmedrs878854632
geneviewrs878854632
scholarrs878854632
googlers878854632
pharmgkbrs878854632
gwascentralrs878854632
openSNPrs878854632
23andMers878854632
23andMe allrs878854632
SNP Nexus

SNPshotrs878854632
SNPdbers878854632
MSV3drs878854632
GWAS Ctlgrs878854632
Max Magnitude0
ClinVar
Risk rs878854632(;)
Alt rs878854632(;)
Reference rs878854632(CAG;CAG)
Significance Probable-Pathogenic
Disease Mitochondrial complex II deficiency Paragangliomas 5
Variation info
Gene SDHA
CLNDBN Mitochondrial complex II deficiency Paragangliomas 5
Reversed 0
HGVS NC_000005.9:g.225996_225998delAGC
CLNSRC
CLNACC RCV000231881.1,