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rs864321644

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864321644(-;-)
Make rs864321644(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position112094876
GeneSDHD
is asnp
is mentioned by
dbSNPrs864321644
dbSNP (classic)rs864321644
ClinGenrs864321644
ebirs864321644
HLIrs864321644
Exacrs864321644
Gnomadrs864321644
Varsomers864321644
LitVarrs864321644
Maprs864321644
PheGenIrs864321644
Biobankrs864321644
1000 genomesrs864321644
hgdprs864321644
ensemblrs864321644
geneviewrs864321644
scholarrs864321644
googlers864321644
pharmgkbrs864321644
gwascentralrs864321644
openSNPrs864321644
23andMers864321644
SNPshotrs864321644
SNPdbers864321644
MSV3drs864321644
GWAS Ctlgrs864321644
Max Magnitude0
ClinVar
Risk rs864321644(-;-)
Alt rs864321644(-;-)
Reference Rs864321644(T;T)
Significance Probable-Pathogenic
Disease Pheochromocytoma
Variation info
Gene SDHD
CLNDBN Pheochromocytoma
Reversed 0
HGVS NC_000011.9:g.111965600delT
CLNSRC Seth G.S. Medical College and K.E.M. Hospital
CLNACC RCV000203535.1,