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rs587776646

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776646(-;-)
Make rs587776646(-;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position112094933
GeneSDHD
is asnp
is mentioned by
dbSNPrs587776646
ebirs587776646
HLIrs587776646
Exacrs587776646
Varsomers587776646
Maprs587776646
PheGenIrs587776646
hapmaprs587776646
1000 genomesrs587776646
hgdprs587776646
ensemblrs587776646
gopubmedrs587776646
geneviewrs587776646
scholarrs587776646
googlers587776646
pharmgkbrs587776646
gwascentralrs587776646
openSNPrs587776646
23andMers587776646
23andMe allrs587776646
SNP Nexus

SNPshotrs587776646
SNPdbers587776646
MSV3drs587776646
GWAS Ctlgrs587776646
Max Magnitude0
ClinVar
Risk rs587776646(;)
Alt rs587776646(;)
Reference rs587776646(G;G)
Significance Pathogenic
Disease Paragangliomas 1
Variation info
Gene SDHD
CLNDBN Paragangliomas 1
Reversed 0
HGVS NC_000011.9:g.111965657delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000007311.3,