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rs1060503770

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060503770(C;T)
Make rs1060503770(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position112094815
GeneSDHD
is asnp
is mentioned by
dbSNPrs1060503770
dbSNP (old)rs1060503770
ClinGenrs1060503770
ebirs1060503770
HLIrs1060503770
Exacrs1060503770
Gnomadrs1060503770
Varsomers1060503770
Maprs1060503770
PheGenIrs1060503770
Biobankrs1060503770
1000 genomesrs1060503770
hgdprs1060503770
ensemblrs1060503770
gopubmedrs1060503770
geneviewrs1060503770
scholarrs1060503770
googlers1060503770
pharmgkbrs1060503770
gwascentralrs1060503770
openSNPrs1060503770
23andMers1060503770
23andMe allrs1060503770
SNPshotrs1060503770
SNPdbers1060503770
MSV3drs1060503770
GWAS Ctlgrs1060503770
Max Magnitude0
ClinVar
Risk rs1060503770(T;T)
Alt rs1060503770(T;T)
Reference Rs1060503770(C;C)
Significance Pathogenic
Disease Paragangliomas 1 Pheochromocytoma Hereditary cancer-predisposing syndrome
Variation info
Gene SDHD
CLNDBN Paragangliomas 1 Pheochromocytoma Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.111965539C>T
CLNSRC
CLNACC RCV000456537.1, RCV000492697.1,