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rs730881956

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730881956(-;-)
Make rs730881956(-;CG)
Make rs730881956(CG;CG)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position51067138
GeneSMAD4
is asnp
is mentioned by
dbSNPrs730881956
ebirs730881956
HLIrs730881956
Exacrs730881956
Varsomers730881956
Maprs730881956
PheGenIrs730881956
hapmaprs730881956
1000 genomesrs730881956
hgdprs730881956
ensemblrs730881956
gopubmedrs730881956
geneviewrs730881956
scholarrs730881956
googlers730881956
pharmgkbrs730881956
gwascentralrs730881956
openSNPrs730881956
23andMers730881956
23andMe allrs730881956
SNP Nexus

SNPshotrs730881956
SNPdbers730881956
MSV3drs730881956
GWAS Ctlgrs730881956
Max Magnitude0
ClinVar
Risk rs730881956(GC;GC)
Alt rs730881956(GC;GC)
Reference rs730881956(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene SMAD4
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000018.9:g.48593507_48593508dupCG
CLNSRC
CLNACC RCV000160965.1,