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rs863223815

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223815(C;C)
Make rs863223815(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position99138042
GeneTGFBR1
is asnp
is mentioned by
dbSNPrs863223815
ebirs863223815
HLIrs863223815
Exacrs863223815
Varsomers863223815
Maprs863223815
PheGenIrs863223815
hapmaprs863223815
1000 genomesrs863223815
hgdprs863223815
ensemblrs863223815
gopubmedrs863223815
geneviewrs863223815
scholarrs863223815
googlers863223815
pharmgkbrs863223815
gwascentralrs863223815
openSNPrs863223815
23andMers863223815
23andMe allrs863223815
SNP Nexus

SNPshotrs863223815
SNPdbers863223815
MSV3drs863223815
GWAS Ctlgrs863223815
Max Magnitude0
ClinVar
Risk rs863223815(C;C)
Alt rs863223815(C;C)
Reference rs863223815(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFBR1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.101900324T>C
CLNSRC
CLNACC RCV000197160.1,