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rs863223822

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223822(A;C)
Make rs863223822(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position99144810
GeneTGFBR1
is asnp
is mentioned by
dbSNPrs863223822
ebirs863223822
HLIrs863223822
Exacrs863223822
Varsomers863223822
Maprs863223822
PheGenIrs863223822
hapmaprs863223822
1000 genomesrs863223822
hgdprs863223822
ensemblrs863223822
gopubmedrs863223822
geneviewrs863223822
scholarrs863223822
googlers863223822
pharmgkbrs863223822
gwascentralrs863223822
openSNPrs863223822
23andMers863223822
23andMe allrs863223822
SNP Nexus

SNPshotrs863223822
SNPdbers863223822
MSV3drs863223822
GWAS Ctlgrs863223822
Max Magnitude0
ClinVar
Risk rs863223822(C;C)
Alt rs863223822(C;C)
Reference rs863223822(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFBR1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.101907092A>C
CLNSRC
CLNACC RCV000198106.1,