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rs863223793

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223793(G;T)
Make rs863223793(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position218437363
GeneTGFB2
is asnp
is mentioned by
dbSNPrs863223793
ebirs863223793
HLIrs863223793
Exacrs863223793
Varsomers863223793
Maprs863223793
PheGenIrs863223793
hapmaprs863223793
1000 genomesrs863223793
hgdprs863223793
ensemblrs863223793
gopubmedrs863223793
geneviewrs863223793
scholarrs863223793
googlers863223793
pharmgkbrs863223793
gwascentralrs863223793
openSNPrs863223793
23andMers863223793
23andMe allrs863223793
SNP Nexus

SNPshotrs863223793
SNPdbers863223793
MSV3drs863223793
GWAS Ctlgrs863223793
Max Magnitude0
ClinVar
Risk rs863223793(T;T)
Alt rs863223793(T;T)
Reference rs863223793(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFB2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.218610705G>T
CLNSRC
CLNACC RCV000197949.1,