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rs786201316

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786201316(A;GG)
Make rs786201316(GG;GG)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position17028712
GeneSDHB
is asnp
is mentioned by
dbSNPrs786201316
ebirs786201316
HLIrs786201316
Exacrs786201316
Varsomers786201316
Maprs786201316
PheGenIrs786201316
hapmaprs786201316
1000 genomesrs786201316
hgdprs786201316
ensemblrs786201316
gopubmedrs786201316
geneviewrs786201316
scholarrs786201316
googlers786201316
pharmgkbrs786201316
gwascentralrs786201316
openSNPrs786201316
23andMers786201316
23andMe allrs786201316
SNP Nexus

SNPshotrs786201316
SNPdbers786201316
MSV3drs786201316
GWAS Ctlgrs786201316
Max Magnitude0
ClinVar
Risk rs786201316(GG;GG)
Alt rs786201316(GG;GG)
Reference rs786201316(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene SDHB
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.17355207delTinsCC
CLNSRC
CLNACC RCV000163361.1,