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rs1064796471

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Chromosome18
Position51047056
GeneSMAD4
is asnp
is mentioned by
dbSNPrs1064796471
dbSNP (old)rs1064796471
ClinGenrs1064796471
ebirs1064796471
HLIrs1064796471
Exacrs1064796471
Gnomadrs1064796471
Varsomers1064796471
Maprs1064796471
PheGenIrs1064796471
Biobankrs1064796471
1000 genomesrs1064796471
hgdprs1064796471
ensemblrs1064796471
gopubmedrs1064796471
geneviewrs1064796471
scholarrs1064796471
googlers1064796471
pharmgkbrs1064796471
gwascentralrs1064796471
openSNPrs1064796471
23andMers1064796471
23andMe allrs1064796471
SNPshotrs1064796471
SNPdbers1064796471
MSV3drs1064796471
GWAS Ctlgrs1064796471
Max Magnitude0
ClinVar
Risk rs1064796471(-;-)
Alt rs1064796471(-;-)
Reference Rs1064796471(AT;AT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMAD4
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.48573426_48573427delAT
CLNSRC
CLNACC RCV000478172.1,