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rs863223843

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223843(C;T)
Make rs863223843(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position30672303
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs863223843
ebirs863223843
HLIrs863223843
Exacrs863223843
Varsomers863223843
Maprs863223843
PheGenIrs863223843
hapmaprs863223843
1000 genomesrs863223843
hgdprs863223843
ensemblrs863223843
gopubmedrs863223843
geneviewrs863223843
scholarrs863223843
googlers863223843
pharmgkbrs863223843
gwascentralrs863223843
openSNPrs863223843
23andMers863223843
23andMe allrs863223843
SNP Nexus

SNPshotrs863223843
SNPdbers863223843
MSV3drs863223843
GWAS Ctlgrs863223843
Max Magnitude0
ClinVar
Risk rs863223843(T;T)
Alt rs863223843(T;T)
Reference rs863223843(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFBR2
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.30713795C>T
CLNSRC
CLNACC RCV000196206.1,