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rs1060503752

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs1060503752(-;-)
Make rs1060503752(-;TG)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position17023994
GeneSDHB
is asnp
is mentioned by
dbSNPrs1060503752
dbSNP (old)rs1060503752
ClinGenrs1060503752
ebirs1060503752
HLIrs1060503752
Exacrs1060503752
Gnomadrs1060503752
Varsomers1060503752
Maprs1060503752
PheGenIrs1060503752
Biobankrs1060503752
1000 genomesrs1060503752
hgdprs1060503752
ensemblrs1060503752
gopubmedrs1060503752
geneviewrs1060503752
scholarrs1060503752
googlers1060503752
pharmgkbrs1060503752
gwascentralrs1060503752
openSNPrs1060503752
23andMers1060503752
23andMe allrs1060503752
SNPshotrs1060503752
SNPdbers1060503752
MSV3drs1060503752
GWAS Ctlgrs1060503752
Max Magnitude0
ClinVar
Risk rs1060503752(-;-)
Alt rs1060503752(-;-)
Reference Rs1060503752(TG;TG)
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.17350489_17350490delCA
CLNSRC
CLNACC RCV000471748.1,