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rs863223814

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223814(C;C)
Make rs863223814(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position99138008
GeneTGFBR1
is asnp
is mentioned by
dbSNPrs863223814
ebirs863223814
HLIrs863223814
Exacrs863223814
Varsomers863223814
Maprs863223814
PheGenIrs863223814
hapmaprs863223814
1000 genomesrs863223814
hgdprs863223814
ensemblrs863223814
gopubmedrs863223814
geneviewrs863223814
scholarrs863223814
googlers863223814
pharmgkbrs863223814
gwascentralrs863223814
openSNPrs863223814
23andMers863223814
23andMe allrs863223814
SNP Nexus

SNPshotrs863223814
SNPdbers863223814
MSV3drs863223814
GWAS Ctlgrs863223814
Max Magnitude0
ClinVar
Risk rs863223814(C;C)
Alt rs863223814(C;C)
Reference rs863223814(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFBR1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.101900290T>C
CLNSRC
CLNACC RCV000200391.1,