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rs786203800

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786203800(A;A)
Make rs786203800(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position17053994
GeneSDHB
is asnp
is mentioned by
dbSNPrs786203800
ebirs786203800
HLIrs786203800
Exacrs786203800
Varsomers786203800
Maprs786203800
PheGenIrs786203800
hapmaprs786203800
1000 genomesrs786203800
hgdprs786203800
ensemblrs786203800
gopubmedrs786203800
geneviewrs786203800
scholarrs786203800
googlers786203800
pharmgkbrs786203800
gwascentralrs786203800
openSNPrs786203800
23andMers786203800
23andMe allrs786203800
SNP Nexus

SNPshotrs786203800
SNPdbers786203800
MSV3drs786203800
GWAS Ctlgrs786203800
Max Magnitude0
ClinVar
Risk rs786203800(A;A)
Alt rs786203800(A;A)
Reference rs786203800(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene SDHB
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000001.10:g.17380489A>T
CLNSRC
CLNACC RCV000167262.1,