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rs587776652

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776652(A;A)
Make rs587776652(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position161314408
GeneSDHC
is asnp
is mentioned by
dbSNPrs587776652
ebirs587776652
HLIrs587776652
Exacrs587776652
Varsomers587776652
Maprs587776652
PheGenIrs587776652
hapmaprs587776652
1000 genomesrs587776652
hgdprs587776652
ensemblrs587776652
gopubmedrs587776652
geneviewrs587776652
scholarrs587776652
googlers587776652
pharmgkbrs587776652
gwascentralrs587776652
openSNPrs587776652
23andMers587776652
23andMe allrs587776652
SNP Nexus

SNPshotrs587776652
SNPdbers587776652
MSV3drs587776652
GWAS Ctlgrs587776652
Max Magnitude0
ClinVar
Risk rs587776652(A;A)
Alt rs587776652(A;A)
Reference rs587776652(G;G)
Significance Pathogenic
Disease Paragangliomas 3
Variation info
Gene SDHC
CLNDBN Paragangliomas 3
Reversed 0
HGVS NC_000001.10:g.161284198G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007663.3,