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rs1060503773

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060503773(-;-)
Make rs1060503773(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position112094884
GeneSDHD
is asnp
is mentioned by
dbSNPrs1060503773
dbSNP (old)rs1060503773
ClinGenrs1060503773
ebirs1060503773
HLIrs1060503773
Exacrs1060503773
Gnomadrs1060503773
Varsomers1060503773
Maprs1060503773
PheGenIrs1060503773
Biobankrs1060503773
1000 genomesrs1060503773
hgdprs1060503773
ensemblrs1060503773
gopubmedrs1060503773
geneviewrs1060503773
scholarrs1060503773
googlers1060503773
pharmgkbrs1060503773
gwascentralrs1060503773
openSNPrs1060503773
23andMers1060503773
23andMe allrs1060503773
SNPshotrs1060503773
SNPdbers1060503773
MSV3drs1060503773
GWAS Ctlgrs1060503773
Max Magnitude0
ClinVar
Risk rs1060503773(-;-)
Alt rs1060503773(-;-)
Reference Rs1060503773(T;T)
Significance Probable-Pathogenic
Disease Paragangliomas 1 Pheochromocytoma
Variation info
Gene SDHD
CLNDBN Paragangliomas 1 Pheochromocytoma
Reversed 0
HGVS NC_000011.9:g.111965608delT
CLNSRC
CLNACC RCV000465313.1,