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rs863223831

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223831(A;A)
Make rs863223831(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position99132593
GeneTGFBR1
is asnp
is mentioned by
dbSNPrs863223831
ClinGenrs863223831
ebirs863223831
HLIrs863223831
Exacrs863223831
Varsomers863223831
Maprs863223831
PheGenIrs863223831
hapmaprs863223831
1000 genomesrs863223831
hgdprs863223831
ensemblrs863223831
gopubmedrs863223831
geneviewrs863223831
scholarrs863223831
googlers863223831
pharmgkbrs863223831
gwascentralrs863223831
openSNPrs863223831
23andMers863223831
23andMe allrs863223831
SNP Nexus

SNPshotrs863223831
SNPdbers863223831
MSV3drs863223831
GWAS Ctlgrs863223831
Max Magnitude0
ClinVar
Risk rs863223831(A;A)
Alt rs863223831(A;A)
Reference Rs863223831(T;T)
Significance Pathogenic
Disease not specified
Variation info
Gene TGFBR1
CLNDBN not specified
Reversed 0
HGVS NC_000009.11:g.101894875T>A
CLNSRC
CLNACC RCV000197925.1,