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rs1060503759

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060503759(A;A)
Make rs1060503759(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position17024013
GeneSDHB
is asnp
is mentioned by
dbSNPrs1060503759
dbSNP (old)rs1060503759
ClinGenrs1060503759
ebirs1060503759
HLIrs1060503759
Exacrs1060503759
Gnomadrs1060503759
Varsomers1060503759
Maprs1060503759
PheGenIrs1060503759
Biobankrs1060503759
1000 genomesrs1060503759
hgdprs1060503759
ensemblrs1060503759
gopubmedrs1060503759
geneviewrs1060503759
scholarrs1060503759
googlers1060503759
pharmgkbrs1060503759
gwascentralrs1060503759
openSNPrs1060503759
23andMers1060503759
23andMe allrs1060503759
SNPshotrs1060503759
SNPdbers1060503759
MSV3drs1060503759
GWAS Ctlgrs1060503759
Max Magnitude0
ClinVar
Risk rs1060503759(A;A)
Alt rs1060503759(A;A)
Reference Rs1060503759(G;G)
Significance Pathogenic
Disease Gastrointestinal stromal tumor Paragangliomas 4 Pheochromocytoma
Variation info
Gene SDHB
CLNDBN Gastrointestinal stromal tumor Paragangliomas 4 Pheochromocytoma
Reversed 1
HGVS NC_000001.10:g.17350508C>T
CLNSRC
CLNACC RCV000458792.1,