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rs786203560

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786203560(-;-)
Make rs786203560(-;A)
Make rs786203560(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position51047199
GeneSMAD4
is asnp
is mentioned by
dbSNPrs786203560
ebirs786203560
HLIrs786203560
Exacrs786203560
Varsomers786203560
Maprs786203560
PheGenIrs786203560
hapmaprs786203560
1000 genomesrs786203560
hgdprs786203560
ensemblrs786203560
gopubmedrs786203560
geneviewrs786203560
scholarrs786203560
googlers786203560
pharmgkbrs786203560
gwascentralrs786203560
openSNPrs786203560
23andMers786203560
23andMe allrs786203560
SNP Nexus

SNPshotrs786203560
SNPdbers786203560
MSV3drs786203560
GWAS Ctlgrs786203560
Max Magnitude0
ClinVar
Risk rs786203560(A;A)
Alt rs786203560(A;A)
Reference rs786203560(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene SMAD4
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000018.9:g.48573569dupA
CLNSRC
CLNACC RCV000166924.1,