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rs1060503769

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060503769(A;A)
Make rs1060503769(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position112094805
GeneSDHD
is asnp
is mentioned by
dbSNPrs1060503769
dbSNP (old)rs1060503769
ClinGenrs1060503769
ebirs1060503769
HLIrs1060503769
Exacrs1060503769
Gnomadrs1060503769
Varsomers1060503769
Maprs1060503769
PheGenIrs1060503769
Biobankrs1060503769
1000 genomesrs1060503769
hgdprs1060503769
ensemblrs1060503769
gopubmedrs1060503769
geneviewrs1060503769
scholarrs1060503769
googlers1060503769
pharmgkbrs1060503769
gwascentralrs1060503769
openSNPrs1060503769
23andMers1060503769
23andMe allrs1060503769
SNPshotrs1060503769
SNPdbers1060503769
MSV3drs1060503769
GWAS Ctlgrs1060503769
Max Magnitude0
ClinVar
Risk rs1060503769(A;A)
Alt rs1060503769(A;A)
Reference Rs1060503769(G;G)
Significance Pathogenic
Disease Paragangliomas 1 Pheochromocytoma
Variation info
Gene SDHD
CLNDBN Paragangliomas 1 Pheochromocytoma
Reversed 0
HGVS NC_000011.9:g.111965529G>A
CLNSRC
CLNACC RCV000462080.1,