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rs863223796

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223796(-;A)
Make rs863223796(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position218436036
GeneTGFB2
is asnp
is mentioned by
dbSNPrs863223796
ClinGenrs863223796
ebirs863223796
HLIrs863223796
Exacrs863223796
Varsomers863223796
Maprs863223796
PheGenIrs863223796
hapmaprs863223796
1000 genomesrs863223796
hgdprs863223796
ensemblrs863223796
gopubmedrs863223796
geneviewrs863223796
scholarrs863223796
googlers863223796
pharmgkbrs863223796
gwascentralrs863223796
openSNPrs863223796
23andMers863223796
23andMe allrs863223796
SNP Nexus

SNPshotrs863223796
SNPdbers863223796
MSV3drs863223796
GWAS Ctlgrs863223796
Max Magnitude0
ClinVar
Risk rs863223796(A;A)
Alt rs863223796(A;A)
Reference Rs863223796(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene TGFB2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.218609378dupA
CLNSRC
CLNACC RCV000197799.1,