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rs863223813

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223813(A;G)
Make rs863223813(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position99137993
GeneTGFBR1
is asnp
is mentioned by
dbSNPrs863223813
ebirs863223813
HLIrs863223813
Exacrs863223813
Varsomers863223813
Maprs863223813
PheGenIrs863223813
hapmaprs863223813
1000 genomesrs863223813
hgdprs863223813
ensemblrs863223813
gopubmedrs863223813
geneviewrs863223813
scholarrs863223813
googlers863223813
pharmgkbrs863223813
gwascentralrs863223813
openSNPrs863223813
23andMers863223813
23andMe allrs863223813
SNP Nexus

SNPshotrs863223813
SNPdbers863223813
MSV3drs863223813
GWAS Ctlgrs863223813
Max Magnitude0
ClinVar
Risk rs863223813(G;G)
Alt rs863223813(G;G)
Reference rs863223813(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene TGFBR1
CLNDBN not specified
Reversed 0
HGVS NC_000009.11:g.101900275A>G
CLNSRC
CLNACC RCV000198846.2,