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rs786201200

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786201200(-;-)
Make rs786201200(-;A)
Make rs786201200(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position51067121
GeneSMAD4
is asnp
is mentioned by
dbSNPrs786201200
ebirs786201200
HLIrs786201200
Exacrs786201200
Varsomers786201200
Maprs786201200
PheGenIrs786201200
hapmaprs786201200
1000 genomesrs786201200
hgdprs786201200
ensemblrs786201200
gopubmedrs786201200
geneviewrs786201200
scholarrs786201200
googlers786201200
pharmgkbrs786201200
gwascentralrs786201200
openSNPrs786201200
23andMers786201200
23andMe allrs786201200
SNP Nexus

SNPshotrs786201200
SNPdbers786201200
MSV3drs786201200
GWAS Ctlgrs786201200
Max Magnitude0
ClinVar
Risk rs786201200(A;A)
Alt rs786201200(A;A)
Reference rs786201200(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene SMAD4
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000018.9:g.48593491dupA
CLNSRC
CLNACC RCV000163070.1,