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rs730881954

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881954(A;A)
Make rs730881954(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position51067118
GeneSMAD4
is asnp
is mentioned by
dbSNPrs730881954
ClinGenrs730881954
ebirs730881954
HLIrs730881954
Exacrs730881954
Varsomers730881954
Maprs730881954
PheGenIrs730881954
hapmaprs730881954
1000 genomesrs730881954
hgdprs730881954
ensemblrs730881954
gopubmedrs730881954
geneviewrs730881954
scholarrs730881954
googlers730881954
pharmgkbrs730881954
gwascentralrs730881954
openSNPrs730881954
23andMers730881954
23andMe allrs730881954
SNP Nexus

SNPshotrs730881954
SNPdbers730881954
MSV3drs730881954
GWAS Ctlgrs730881954
Max Magnitude0
ClinVar
Risk rs730881954(A;A)
Alt rs730881954(A;A)
Reference Rs730881954(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SMAD4
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.48593488C>A
CLNSRC
CLNACC RCV000160963.1,