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rs1060503753

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060503753(A;T)
Make rs1060503753(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position17027790
GeneSDHB
is asnp
is mentioned by
dbSNPrs1060503753
dbSNP (old)rs1060503753
ClinGenrs1060503753
ebirs1060503753
HLIrs1060503753
Exacrs1060503753
Gnomadrs1060503753
Varsomers1060503753
LitVarrs1060503753
Maprs1060503753
PheGenIrs1060503753
Biobankrs1060503753
1000 genomesrs1060503753
hgdprs1060503753
ensemblrs1060503753
gopubmedrs1060503753
geneviewrs1060503753
scholarrs1060503753
googlers1060503753
pharmgkbrs1060503753
gwascentralrs1060503753
openSNPrs1060503753
23andMers1060503753
23andMe allrs1060503753
SNPshotrs1060503753
SNPdbers1060503753
MSV3drs1060503753
GWAS Ctlgrs1060503753
Max Magnitude0
ClinVar
Risk rs1060503753(T;T)
Alt rs1060503753(T;T)
Reference Rs1060503753(A;A)
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.17354285T>A
CLNSRC
CLNACC RCV000463782.1,