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rs863223794

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223794(-;-)
Make rs863223794(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position218346897
GeneTGFB2, TGFB2-AS1
is asnp
is mentioned by
dbSNPrs863223794
ClinGenrs863223794
ebirs863223794
HLIrs863223794
Exacrs863223794
Varsomers863223794
Maprs863223794
PheGenIrs863223794
hapmaprs863223794
1000 genomesrs863223794
hgdprs863223794
ensemblrs863223794
gopubmedrs863223794
geneviewrs863223794
scholarrs863223794
googlers863223794
pharmgkbrs863223794
gwascentralrs863223794
openSNPrs863223794
23andMers863223794
23andMe allrs863223794
SNP Nexus

SNPshotrs863223794
SNPdbers863223794
MSV3drs863223794
GWAS Ctlgrs863223794
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs863223794(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TGFB2 TGFB2-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.218520239delG
CLNSRC
CLNACC RCV000200166.1,