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rs730881952

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs730881952(-;-)
Make rs730881952(-;AG)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position51067110
GeneSMAD4
is asnp
is mentioned by
dbSNPrs730881952
ebirs730881952
HLIrs730881952
Exacrs730881952
Varsomers730881952
Maprs730881952
PheGenIrs730881952
hapmaprs730881952
1000 genomesrs730881952
hgdprs730881952
ensemblrs730881952
gopubmedrs730881952
geneviewrs730881952
scholarrs730881952
googlers730881952
pharmgkbrs730881952
gwascentralrs730881952
openSNPrs730881952
23andMers730881952
23andMe allrs730881952
SNP Nexus

SNPshotrs730881952
SNPdbers730881952
MSV3drs730881952
GWAS Ctlgrs730881952
Max Magnitude0
ClinVar
Risk rs730881952(;)
Alt rs730881952(;)
Reference rs730881952(AG;AG)
Significance Pathogenic
Disease not provided
Variation info
Gene SMAD4
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.48593480_48593481delAG
CLNSRC
CLNACC RCV000160956.2,