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rs786202403

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786202403(A;A)
Make rs786202403(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position112089001
GeneSDHD
is asnp
is mentioned by
dbSNPrs786202403
ebirs786202403
HLIrs786202403
Exacrs786202403
Varsomers786202403
Maprs786202403
PheGenIrs786202403
hapmaprs786202403
1000 genomesrs786202403
hgdprs786202403
ensemblrs786202403
gopubmedrs786202403
geneviewrs786202403
scholarrs786202403
googlers786202403
pharmgkbrs786202403
gwascentralrs786202403
openSNPrs786202403
23andMers786202403
23andMe allrs786202403
SNP Nexus

SNPshotrs786202403
SNPdbers786202403
MSV3drs786202403
GWAS Ctlgrs786202403
Max Magnitude0
ClinVar
Risk rs786202403(A;A)
Alt rs786202403(A;A)
Reference rs786202403(C;C)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene SDHD
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.111959725C>A
CLNSRC
CLNACC RCV000165195.1,