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rs1060503767

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs1060503767(-;-)
Make rs1060503767(-;TC)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position17053997
GeneSDHB
is asnp
is mentioned by
dbSNPrs1060503767
dbSNP (old)rs1060503767
ClinGenrs1060503767
ebirs1060503767
HLIrs1060503767
Exacrs1060503767
Gnomadrs1060503767
Varsomers1060503767
Maprs1060503767
PheGenIrs1060503767
Biobankrs1060503767
1000 genomesrs1060503767
hgdprs1060503767
ensemblrs1060503767
gopubmedrs1060503767
geneviewrs1060503767
scholarrs1060503767
googlers1060503767
pharmgkbrs1060503767
gwascentralrs1060503767
openSNPrs1060503767
23andMers1060503767
23andMe allrs1060503767
SNPshotrs1060503767
SNPdbers1060503767
MSV3drs1060503767
GWAS Ctlgrs1060503767
Max Magnitude0
ClinVar
Risk rs1060503767(-;-)
Alt rs1060503767(-;-)
Reference Rs1060503767(TC;TC)
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.17380492_17380493delGA
CLNSRC
CLNACC RCV000464374.1,