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rs863223848

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223848(A;A)
Make rs863223848(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position30674106
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs863223848
ebirs863223848
HLIrs863223848
Exacrs863223848
Varsomers863223848
Maprs863223848
PheGenIrs863223848
hapmaprs863223848
1000 genomesrs863223848
hgdprs863223848
ensemblrs863223848
gopubmedrs863223848
geneviewrs863223848
scholarrs863223848
googlers863223848
pharmgkbrs863223848
gwascentralrs863223848
openSNPrs863223848
23andMers863223848
23andMe allrs863223848
SNP Nexus

SNPshotrs863223848
SNPdbers863223848
MSV3drs863223848
GWAS Ctlgrs863223848
Max Magnitude0
ClinVar
Risk rs863223848(A;A)
Alt rs863223848(A;A)
Reference rs863223848(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFBR2
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.30715598T>A
CLNSRC
CLNACC RCV000200367.1,