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rs1060503763

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060503763(G;G)
Make rs1060503763(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position17027848
GeneSDHB
is asnp
is mentioned by
dbSNPrs1060503763
dbSNP (classic)rs1060503763
ClinGenrs1060503763
ebirs1060503763
HLIrs1060503763
Exacrs1060503763
Gnomadrs1060503763
Varsomers1060503763
LitVarrs1060503763
Maprs1060503763
PheGenIrs1060503763
Biobankrs1060503763
1000 genomesrs1060503763
hgdprs1060503763
ensemblrs1060503763
geneviewrs1060503763
scholarrs1060503763
googlers1060503763
pharmgkbrs1060503763
gwascentralrs1060503763
openSNPrs1060503763
23andMers1060503763
23andMe allrs1060503763
SNPshotrs1060503763
SNPdbers1060503763
MSV3drs1060503763
GWAS Ctlgrs1060503763
Max Magnitude0
ClinVar
Risk rs1060503763(G;G)
Alt rs1060503763(G;G)
Reference Rs1060503763(T;T)
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.17354343A>C
CLNSRC
CLNACC RCV000460882.1,