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rs786205210

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205210(A;G)
Make rs786205210(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position240474
GeneSDHA
is asnp
is mentioned by
dbSNPrs786205210
ebirs786205210
HLIrs786205210
Exacrs786205210
Varsomers786205210
Maprs786205210
PheGenIrs786205210
hapmaprs786205210
1000 genomesrs786205210
hgdprs786205210
ensemblrs786205210
gopubmedrs786205210
geneviewrs786205210
scholarrs786205210
googlers786205210
pharmgkbrs786205210
gwascentralrs786205210
openSNPrs786205210
23andMers786205210
23andMe allrs786205210
SNP Nexus

SNPshotrs786205210
SNPdbers786205210
MSV3drs786205210
GWAS Ctlgrs786205210
Max Magnitude0
ClinVar
Risk rs786205210(G;G)
Alt rs786205210(G;G)
Reference rs786205210(A;A)
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.240589A>G
CLNSRC
CLNACC RCV000170440.1, RCV000231483.1,