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rs863223850

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223850(C;T)
Make rs863223850(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position30674129
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs863223850
ebirs863223850
HLIrs863223850
Exacrs863223850
Varsomers863223850
Maprs863223850
PheGenIrs863223850
hapmaprs863223850
1000 genomesrs863223850
hgdprs863223850
ensemblrs863223850
gopubmedrs863223850
geneviewrs863223850
scholarrs863223850
googlers863223850
pharmgkbrs863223850
gwascentralrs863223850
openSNPrs863223850
23andMers863223850
23andMe allrs863223850
SNP Nexus

SNPshotrs863223850
SNPdbers863223850
MSV3drs863223850
GWAS Ctlgrs863223850
Max Magnitude0
ClinVar
Risk rs863223850(T;T)
Alt rs863223850(T;T)
Reference rs863223850(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TGFBR2
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.30715621C>T
CLNSRC
CLNACC RCV000195460.1,