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rs863223842

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223842(A;G)
Make rs863223842(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position30672268
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs863223842
ebirs863223842
HLIrs863223842
Exacrs863223842
Varsomers863223842
Maprs863223842
PheGenIrs863223842
hapmaprs863223842
1000 genomesrs863223842
hgdprs863223842
ensemblrs863223842
gopubmedrs863223842
geneviewrs863223842
scholarrs863223842
googlers863223842
pharmgkbrs863223842
gwascentralrs863223842
openSNPrs863223842
23andMers863223842
23andMe allrs863223842
SNP Nexus

SNPshotrs863223842
SNPdbers863223842
MSV3drs863223842
GWAS Ctlgrs863223842
Max Magnitude0
ClinVar
Risk rs863223842(G;G)
Alt rs863223842(G;G)
Reference rs863223842(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFBR2
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.30713760A>G
CLNSRC
CLNACC RCV000200101.1,