Have questions? Visit https://www.reddit.com/r/SNPedia

rs746165168

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs746165168(A;A)
Make rs746165168(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position233635
GeneSDHA
is asnp
is mentioned by
dbSNPrs746165168
ebirs746165168
HLIrs746165168
Exacrs746165168
Varsomers746165168
Maprs746165168
PheGenIrs746165168
hapmaprs746165168
1000 genomesrs746165168
hgdprs746165168
ensemblrs746165168
gopubmedrs746165168
geneviewrs746165168
scholarrs746165168
googlers746165168
pharmgkbrs746165168
gwascentralrs746165168
openSNPrs746165168
23andMers746165168
23andMe allrs746165168
SNP Nexus

SNPshotrs746165168
SNPdbers746165168
MSV3drs746165168
GWAS Ctlgrs746165168
Max Magnitude0
ClinVar
Risk rs746165168(A;A)
Alt rs746165168(A;A)
Reference rs746165168(C;C)
Significance 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.233750C>T
CLNSRC
CLNACC RCV000232152.1,