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rs863223841

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223841(A;A)
Make rs863223841(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position30672181
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs863223841
ebirs863223841
HLIrs863223841
Exacrs863223841
Varsomers863223841
Maprs863223841
PheGenIrs863223841
hapmaprs863223841
1000 genomesrs863223841
hgdprs863223841
ensemblrs863223841
gopubmedrs863223841
geneviewrs863223841
scholarrs863223841
googlers863223841
pharmgkbrs863223841
gwascentralrs863223841
openSNPrs863223841
23andMers863223841
23andMe allrs863223841
SNP Nexus

SNPshotrs863223841
SNPdbers863223841
MSV3drs863223841
GWAS Ctlgrs863223841
Max Magnitude0
ClinVar
Risk rs863223841(A;A)
Alt rs863223841(A;A)
Reference rs863223841(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFBR2
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.30713673T>A
CLNSRC
CLNACC RCV000199560.1,