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rs797044882

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044882(C;C)
Make rs797044882(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position47848537
GeneSMAD2
is asnp
is mentioned by
dbSNPrs797044882
ebirs797044882
HLIrs797044882
Exacrs797044882
Varsomers797044882
Maprs797044882
PheGenIrs797044882
hapmaprs797044882
1000 genomesrs797044882
hgdprs797044882
ensemblrs797044882
gopubmedrs797044882
geneviewrs797044882
scholarrs797044882
googlers797044882
pharmgkbrs797044882
gwascentralrs797044882
openSNPrs797044882
23andMers797044882
23andMe allrs797044882
SNP Nexus

SNPshotrs797044882
SNPdbers797044882
MSV3drs797044882
GWAS Ctlgrs797044882
Max Magnitude0
ClinVar
Risk rs797044882(C;C)
Alt rs797044882(C;C)
Reference rs797044882(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene SMAD2
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000018.9:g.45374908C>G
CLNSRC
CLNACC RCV000190697.1,