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rs587776647

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587776647(-;-)
Make rs587776647(-;A)
ReferenceGRCh38 38.1/142
Chromosome11
Position112094953
GeneSDHD
is asnp
is mentioned by
dbSNPrs587776647
ebirs587776647
HLIrs587776647
Exacrs587776647
Varsomers587776647
Maprs587776647
PheGenIrs587776647
hapmaprs587776647
1000 genomesrs587776647
hgdprs587776647
ensemblrs587776647
gopubmedrs587776647
geneviewrs587776647
scholarrs587776647
googlers587776647
pharmgkbrs587776647
gwascentralrs587776647
openSNPrs587776647
23andMers587776647
23andMe allrs587776647
SNP Nexus

SNPshotrs587776647
SNPdbers587776647
MSV3drs587776647
GWAS Ctlgrs587776647
Max Magnitude0
ClinVar
Risk rs587776647(;)
Alt rs587776647(;)
Reference rs587776647(A;A)
Significance Pathogenic
Disease Paragangliomas 1
Variation info
Gene SDHD
CLNDBN Paragangliomas 1
Reversed 0
HGVS NC_000011.9:g.111965677delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000007319.2,