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rs587782077

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587782077(-;-)
Make rs587782077(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position228230
GeneSDHA
is asnp
is mentioned by
dbSNPrs587782077
ebirs587782077
HLIrs587782077
Exacrs587782077
Varsomers587782077
Maprs587782077
PheGenIrs587782077
hapmaprs587782077
1000 genomesrs587782077
hgdprs587782077
ensemblrs587782077
gopubmedrs587782077
geneviewrs587782077
scholarrs587782077
googlers587782077
pharmgkbrs587782077
gwascentralrs587782077
openSNPrs587782077
23andMers587782077
23andMe allrs587782077
SNP Nexus

SNPshotrs587782077
SNPdbers587782077
MSV3drs587782077
GWAS Ctlgrs587782077
Max Magnitude0
ClinVar
Risk rs587782077(;)
Alt rs587782077(;)
Reference rs587782077(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene SDHA
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.228345delG
CLNSRC
CLNACC RCV000130573.2,