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rs863223856

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223856(C;T)
Make rs863223856(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position30671943
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs863223856
ebirs863223856
HLIrs863223856
Exacrs863223856
Varsomers863223856
Maprs863223856
PheGenIrs863223856
hapmaprs863223856
1000 genomesrs863223856
hgdprs863223856
ensemblrs863223856
gopubmedrs863223856
geneviewrs863223856
scholarrs863223856
googlers863223856
pharmgkbrs863223856
gwascentralrs863223856
openSNPrs863223856
23andMers863223856
23andMe allrs863223856
SNP Nexus

SNPshotrs863223856
SNPdbers863223856
MSV3drs863223856
GWAS Ctlgrs863223856
Max Magnitude0
ClinVar
Risk rs863223856(T;T)
Alt rs863223856(T;T)
Reference rs863223856(C;C)
Significance Pathogenic
Disease not specified
Variation info
Gene TGFBR2
CLNDBN not specified
Reversed 0
HGVS NC_000003.11:g.30713435C>T
CLNSRC
CLNACC RCV000198902.2,