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rs1057519741

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519741(G;T)
Make rs1057519741(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position51078417
GeneSMAD4
is asnp
is mentioned by
dbSNPrs1057519741
dbSNP (old)rs1057519741
ClinGenrs1057519741
ebirs1057519741
HLIrs1057519741
Exacrs1057519741
Gnomadrs1057519741
Varsomers1057519741
LitVarrs1057519741
Maprs1057519741
PheGenIrs1057519741
Biobankrs1057519741
1000 genomesrs1057519741
hgdprs1057519741
ensemblrs1057519741
gopubmedrs1057519741
geneviewrs1057519741
scholarrs1057519741
googlers1057519741
pharmgkbrs1057519741
gwascentralrs1057519741
openSNPrs1057519741
23andMers1057519741
23andMe allrs1057519741
SNPshotrs1057519741
SNPdbers1057519741
MSV3drs1057519741
GWAS Ctlgrs1057519741
Max Magnitude0
ClinVar
Risk rs1057519741(T;T)
Alt rs1057519741(T;T)
Reference Rs1057519741(G;G)
Significance Pathogenic
Disease Colorectal Neoplasms
Variation info
Gene SMAD4
CLNDBN Colorectal Neoplasms
Reversed 0
HGVS NC_000018.9:g.48604787G>T
CLNSRC
CLNACC RCV000444970.1,