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rs1060503762

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060503762(A;A)
Make rs1060503762(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position17044820
GeneSDHB
is asnp
is mentioned by
dbSNPrs1060503762
dbSNP (old)rs1060503762
ClinGenrs1060503762
ebirs1060503762
HLIrs1060503762
Exacrs1060503762
Gnomadrs1060503762
Varsomers1060503762
Maprs1060503762
PheGenIrs1060503762
Biobankrs1060503762
1000 genomesrs1060503762
hgdprs1060503762
ensemblrs1060503762
gopubmedrs1060503762
geneviewrs1060503762
scholarrs1060503762
googlers1060503762
pharmgkbrs1060503762
gwascentralrs1060503762
openSNPrs1060503762
23andMers1060503762
23andMe allrs1060503762
SNPshotrs1060503762
SNPdbers1060503762
MSV3drs1060503762
GWAS Ctlgrs1060503762
Max Magnitude0
ClinVar
Risk rs1060503762(A;A)
Alt rs1060503762(A;A)
Reference Rs1060503762(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.17371315C>T
CLNSRC
CLNACC RCV000474236.1,