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rs786203251

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786203251(C;T)
Make rs786203251(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position17022649
GeneSDHB
is asnp
is mentioned by
dbSNPrs786203251
ebirs786203251
HLIrs786203251
Exacrs786203251
Varsomers786203251
Maprs786203251
PheGenIrs786203251
hapmaprs786203251
1000 genomesrs786203251
hgdprs786203251
ensemblrs786203251
gopubmedrs786203251
geneviewrs786203251
scholarrs786203251
googlers786203251
pharmgkbrs786203251
gwascentralrs786203251
openSNPrs786203251
23andMers786203251
23andMe allrs786203251
SNP Nexus

SNPshotrs786203251
SNPdbers786203251
MSV3drs786203251
GWAS Ctlgrs786203251
Max Magnitude0
ClinVar
Risk rs786203251(T;T)
Alt rs786203251(T;T)
Reference rs786203251(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Gastrointestinal stromal tumor Paragangliomas 4 Pheochromocytoma
Variation info
Gene SDHB
CLNDBN Hereditary cancer-predisposing syndrome Gastrointestinal stromal tumor Paragangliomas 4 Pheochromocytoma
Reversed 1
HGVS NC_000001.10:g.17349144G>A; NC_000001.10:g.17349144G>T
CLNSRC
CLNACC RCV000166478.1, RCV000226466.1,