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rs786203067

From SNPedia

Orientationplus
Geno Mag Summary
(CTCA;CTCA) 0 common in clinvar
Make rs786203067(-;-)
Make rs786203067(-;ACTC)
Make rs786203067(ACTC;ACTC)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position112088995
GeneSDHD
is asnp
is mentioned by
dbSNPrs786203067
ebirs786203067
HLIrs786203067
Exacrs786203067
Varsomers786203067
Maprs786203067
PheGenIrs786203067
hapmaprs786203067
1000 genomesrs786203067
hgdprs786203067
ensemblrs786203067
gopubmedrs786203067
geneviewrs786203067
scholarrs786203067
googlers786203067
pharmgkbrs786203067
gwascentralrs786203067
openSNPrs786203067
23andMers786203067
23andMe allrs786203067
SNP Nexus

SNPshotrs786203067
SNPdbers786203067
MSV3drs786203067
GWAS Ctlgrs786203067
Max Magnitude0
ClinVar
Risk rs786203067(;)
Alt rs786203067(;)
Reference rs786203067(CTCA;CTCA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene SDHD
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.111959719_111959722delACTC
CLNSRC
CLNACC RCV000166207.1,