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rs587776648

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ACTG;ACTG) 0 common in clinvar
Make rs587776648(-;-)
Make rs587776648(-;GACT)
Make rs587776648(GACT;GACT)
ReferenceGRCh38 38.1/142
Chromosome11
Position112094827
GeneSDHD
is asnp
is mentioned by
dbSNPrs587776648
ebirs587776648
HLIrs587776648
Exacrs587776648
Varsomers587776648
Maprs587776648
PheGenIrs587776648
hapmaprs587776648
1000 genomesrs587776648
hgdprs587776648
ensemblrs587776648
gopubmedrs587776648
geneviewrs587776648
scholarrs587776648
googlers587776648
pharmgkbrs587776648
gwascentralrs587776648
openSNPrs587776648
23andMers587776648
23andMe allrs587776648
SNP Nexus

SNPshotrs587776648
SNPdbers587776648
MSV3drs587776648
GWAS Ctlgrs587776648
Max Magnitude0
ClinVar
Risk rs587776648(;)
Alt rs587776648(;)
Reference rs587776648(ACTG;ACTG)
Significance Pathogenic
Disease Paragangliomas 1
Variation info
Gene SDHD
CLNDBN Paragangliomas 1
Reversed 0
HGVS NC_000011.9:g.111965551_111965554delGACT
CLNSRC OMIM Allelic Variant
CLNACC RCV000007321.2,