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rs863223808

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223808(C;C)
Make rs863223808(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position99137898
GeneTGFBR1
is asnp
is mentioned by
dbSNPrs863223808
ebirs863223808
HLIrs863223808
Exacrs863223808
Varsomers863223808
Maprs863223808
PheGenIrs863223808
hapmaprs863223808
1000 genomesrs863223808
hgdprs863223808
ensemblrs863223808
gopubmedrs863223808
geneviewrs863223808
scholarrs863223808
googlers863223808
pharmgkbrs863223808
gwascentralrs863223808
openSNPrs863223808
23andMers863223808
23andMe allrs863223808
SNP Nexus

SNPshotrs863223808
SNPdbers863223808
MSV3drs863223808
GWAS Ctlgrs863223808
Max Magnitude0
ClinVar
Risk rs863223808(C;C)
Alt rs863223808(C;C)
Reference rs863223808(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFBR1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.101900180T>C
CLNSRC
CLNACC RCV000200667.1,