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rs863223828

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223828(A;C)
Make rs863223828(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position99149259
GeneTGFBR1
is asnp
is mentioned by
dbSNPrs863223828
ebirs863223828
HLIrs863223828
Exacrs863223828
Varsomers863223828
Maprs863223828
PheGenIrs863223828
hapmaprs863223828
1000 genomesrs863223828
hgdprs863223828
ensemblrs863223828
gopubmedrs863223828
geneviewrs863223828
scholarrs863223828
googlers863223828
pharmgkbrs863223828
gwascentralrs863223828
openSNPrs863223828
23andMers863223828
23andMe allrs863223828
SNP Nexus

SNPshotrs863223828
SNPdbers863223828
MSV3drs863223828
GWAS Ctlgrs863223828
Max Magnitude0
ClinVar
Risk rs863223828(C;C)
Alt rs863223828(C;C)
Reference rs863223828(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFBR1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.101911541A>C
CLNSRC
CLNACC RCV000199055.1,