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rs863223790

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223790(G;T)
Make rs863223790(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position218434154
GeneTGFB2
is asnp
is mentioned by
dbSNPrs863223790
ebirs863223790
HLIrs863223790
Exacrs863223790
Varsomers863223790
Maprs863223790
PheGenIrs863223790
hapmaprs863223790
1000 genomesrs863223790
hgdprs863223790
ensemblrs863223790
gopubmedrs863223790
geneviewrs863223790
scholarrs863223790
googlers863223790
pharmgkbrs863223790
gwascentralrs863223790
openSNPrs863223790
23andMers863223790
23andMe allrs863223790
SNP Nexus

SNPshotrs863223790
SNPdbers863223790
MSV3drs863223790
GWAS Ctlgrs863223790
Max Magnitude0
ClinVar
Risk rs863223790(T;T)
Alt rs863223790(T;T)
Reference rs863223790(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TGFB2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.218607496G>T
CLNSRC
CLNACC RCV000199064.1,