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rs863223812

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223812(C;T)
Make rs863223812(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position99137991
GeneTGFBR1
is asnp
is mentioned by
dbSNPrs863223812
ebirs863223812
HLIrs863223812
Exacrs863223812
Varsomers863223812
Maprs863223812
PheGenIrs863223812
hapmaprs863223812
1000 genomesrs863223812
hgdprs863223812
ensemblrs863223812
gopubmedrs863223812
geneviewrs863223812
scholarrs863223812
googlers863223812
pharmgkbrs863223812
gwascentralrs863223812
openSNPrs863223812
23andMers863223812
23andMe allrs863223812
SNP Nexus

SNPshotrs863223812
SNPdbers863223812
MSV3drs863223812
GWAS Ctlgrs863223812
Max Magnitude0
ClinVar
Risk rs863223812(T;T)
Alt rs863223812(T;T)
Reference rs863223812(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFBR1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.101900273C>T
CLNSRC
CLNACC RCV000197297.1,