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rs1060503757

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060503757(-;-)
Make rs1060503757(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position17024024
GeneSDHB
is asnp
is mentioned by
dbSNPrs1060503757
dbSNP (classic)rs1060503757
ClinGenrs1060503757
ebirs1060503757
HLIrs1060503757
Exacrs1060503757
Gnomadrs1060503757
Varsomers1060503757
LitVarrs1060503757
Maprs1060503757
PheGenIrs1060503757
Biobankrs1060503757
1000 genomesrs1060503757
hgdprs1060503757
ensemblrs1060503757
geneviewrs1060503757
scholarrs1060503757
googlers1060503757
pharmgkbrs1060503757
gwascentralrs1060503757
openSNPrs1060503757
23andMers1060503757
23andMe allrs1060503757
SNPshotrs1060503757
SNPdbers1060503757
MSV3drs1060503757
GWAS Ctlgrs1060503757
Max Magnitude0
ClinVar
Risk rs1060503757(-;-)
Alt rs1060503757(-;-)
Reference Rs1060503757(C;C)
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.17350519delG
CLNSRC
CLNACC RCV000473527.1,