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rs863223795

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223795(-;T)
Make rs863223795(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position218434338
GeneTGFB2
is asnp
is mentioned by
dbSNPrs863223795
ClinGenrs863223795
ebirs863223795
HLIrs863223795
Exacrs863223795
Varsomers863223795
Maprs863223795
PheGenIrs863223795
hapmaprs863223795
1000 genomesrs863223795
hgdprs863223795
ensemblrs863223795
gopubmedrs863223795
geneviewrs863223795
scholarrs863223795
googlers863223795
pharmgkbrs863223795
gwascentralrs863223795
openSNPrs863223795
23andMers863223795
23andMe allrs863223795
SNP Nexus

SNPshotrs863223795
SNPdbers863223795
MSV3drs863223795
GWAS Ctlgrs863223795
Max Magnitude0
ClinVar
Risk rs863223795(T;T)
Alt rs863223795(T;T)
Reference Rs863223795(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene TGFB2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.218607680_218607681insT
CLNSRC
CLNACC RCV000195595.1,