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rs1057519740

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519740(A;A)
Make rs1057519740(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position51065532
GeneSMAD4
is asnp
is mentioned by
dbSNPrs1057519740
dbSNP (old)rs1057519740
ClinGenrs1057519740
ebirs1057519740
HLIrs1057519740
Exacrs1057519740
Gnomadrs1057519740
Varsomers1057519740
Maprs1057519740
PheGenIrs1057519740
Biobankrs1057519740
1000 genomesrs1057519740
hgdprs1057519740
ensemblrs1057519740
gopubmedrs1057519740
geneviewrs1057519740
scholarrs1057519740
googlers1057519740
pharmgkbrs1057519740
gwascentralrs1057519740
openSNPrs1057519740
23andMers1057519740
23andMe allrs1057519740
SNPshotrs1057519740
SNPdbers1057519740
MSV3drs1057519740
GWAS Ctlgrs1057519740
Max Magnitude0
ClinVar
Risk rs1057519740(A;A)
Alt rs1057519740(A;A)
Reference Rs1057519740(C;C)
Significance Pathogenic
Disease Colorectal Neoplasms
Variation info
Gene SMAD4
CLNDBN Colorectal Neoplasms
Reversed 0
HGVS NC_000018.9:g.48591902C>A
CLNSRC
CLNACC RCV000435575.1,