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rs863223817

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223817(A;G)
Make rs863223817(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position99142554
GeneTGFBR1
is asnp
is mentioned by
dbSNPrs863223817
ebirs863223817
HLIrs863223817
Exacrs863223817
Varsomers863223817
Maprs863223817
PheGenIrs863223817
hapmaprs863223817
1000 genomesrs863223817
hgdprs863223817
ensemblrs863223817
gopubmedrs863223817
geneviewrs863223817
scholarrs863223817
googlers863223817
pharmgkbrs863223817
gwascentralrs863223817
openSNPrs863223817
23andMers863223817
23andMe allrs863223817
SNP Nexus

SNPshotrs863223817
SNPdbers863223817
MSV3drs863223817
GWAS Ctlgrs863223817
Max Magnitude0
ClinVar
Risk rs863223817(G;G)
Alt rs863223817(G;G)
Reference rs863223817(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFBR1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.101904836A>G
CLNSRC
CLNACC RCV000195485.1,