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

rs587776645

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776645(-;-)
Make rs587776645(-;T)
Make rs587776645(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position112094827
GeneSDHD
is asnp
is mentioned by
dbSNPrs587776645
ebirs587776645
HLIrs587776645
Exacrs587776645
Varsomers587776645
Maprs587776645
PheGenIrs587776645
hapmaprs587776645
1000 genomesrs587776645
hgdprs587776645
ensemblrs587776645
gopubmedrs587776645
geneviewrs587776645
scholarrs587776645
googlers587776645
pharmgkbrs587776645
gwascentralrs587776645
openSNPrs587776645
23andMers587776645
23andMe allrs587776645
SNP Nexus

SNPshotrs587776645
SNPdbers587776645
MSV3drs587776645
GWAS Ctlgrs587776645
Max Magnitude0
ClinVar
Risk rs587776645(T;T)
Alt rs587776645(T;T)
Reference rs587776645(;)
Significance Pathogenic
Disease Paragangliomas 1
Variation info
Gene SDHD
CLNDBN Paragangliomas 1
Reversed 0
HGVS NC_000011.9:g.111965551_111965552insT
CLNSRC OMIM Allelic Variant
CLNACC RCV000007308.2,