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rs587781618

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781618(G;T)
Make rs587781618(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position51067188
GeneSMAD4
is asnp
is mentioned by
dbSNPrs587781618
ebirs587781618
HLIrs587781618
Exacrs587781618
Varsomers587781618
Maprs587781618
PheGenIrs587781618
hapmaprs587781618
1000 genomesrs587781618
hgdprs587781618
ensemblrs587781618
gopubmedrs587781618
geneviewrs587781618
scholarrs587781618
googlers587781618
pharmgkbrs587781618
gwascentralrs587781618
openSNPrs587781618
23andMers587781618
23andMe allrs587781618
SNP Nexus

SNPshotrs587781618
SNPdbers587781618
MSV3drs587781618
GWAS Ctlgrs587781618
Max Magnitude0
ClinVar
Risk rs587781618(T;T)
Alt rs587781618(T;T)
Reference rs587781618(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene SMAD4
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000018.9:g.48593558G>T
CLNSRC
CLNACC RCV000129707.2,