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rs878854627

From SNPedia

Orientationplus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs878854627(-;-)
Make rs878854627(-;GG)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position236599
GeneSDHA
is asnp
is mentioned by
dbSNPrs878854627
ebirs878854627
HLIrs878854627
Exacrs878854627
Varsomers878854627
Maprs878854627
PheGenIrs878854627
hapmaprs878854627
1000 genomesrs878854627
hgdprs878854627
ensemblrs878854627
gopubmedrs878854627
geneviewrs878854627
scholarrs878854627
googlers878854627
pharmgkbrs878854627
gwascentralrs878854627
openSNPrs878854627
23andMers878854627
23andMe allrs878854627
SNP Nexus

SNPshotrs878854627
SNPdbers878854627
MSV3drs878854627
GWAS Ctlgrs878854627
Max Magnitude0
ClinVar
Risk rs878854627(;)
Alt rs878854627(;)
Reference rs878854627(GG;GG)
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.236714_236715delGG
CLNSRC
CLNACC RCV000228421.1,