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rs863223851

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223851(G;G)
Make rs863223851(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position30674188
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs863223851
ebirs863223851
HLIrs863223851
Exacrs863223851
Varsomers863223851
Maprs863223851
PheGenIrs863223851
hapmaprs863223851
1000 genomesrs863223851
hgdprs863223851
ensemblrs863223851
gopubmedrs863223851
geneviewrs863223851
scholarrs863223851
googlers863223851
pharmgkbrs863223851
gwascentralrs863223851
openSNPrs863223851
23andMers863223851
23andMe allrs863223851
SNP Nexus

SNPshotrs863223851
SNPdbers863223851
MSV3drs863223851
GWAS Ctlgrs863223851
Max Magnitude0
ClinVar
Risk rs863223851(G;G)
Alt rs863223851(G;G)
Reference rs863223851(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFBR2
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.30715680T>G
CLNSRC
CLNACC RCV000197000.1,