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rs786205514

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205514(C;T)
Make rs786205514(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position51076687
GeneSMAD4
is asnp
is mentioned by
dbSNPrs786205514
ebirs786205514
HLIrs786205514
Exacrs786205514
Varsomers786205514
Maprs786205514
PheGenIrs786205514
hapmaprs786205514
1000 genomesrs786205514
hgdprs786205514
ensemblrs786205514
gopubmedrs786205514
geneviewrs786205514
scholarrs786205514
googlers786205514
pharmgkbrs786205514
gwascentralrs786205514
openSNPrs786205514
23andMers786205514
23andMe allrs786205514
SNP Nexus

SNPshotrs786205514
SNPdbers786205514
MSV3drs786205514
GWAS Ctlgrs786205514
Max Magnitude0
ClinVar
Risk rs786205514(T;T)
Alt rs786205514(T;T)
Reference rs786205514(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMAD4
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.48603057C>T
CLNSRC
CLNACC RCV000171276.1,