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rs863223857

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223857(A;G)
Make rs863223857(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position30672085
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs863223857
ebirs863223857
HLIrs863223857
Exacrs863223857
Varsomers863223857
Maprs863223857
PheGenIrs863223857
hapmaprs863223857
1000 genomesrs863223857
hgdprs863223857
ensemblrs863223857
gopubmedrs863223857
geneviewrs863223857
scholarrs863223857
googlers863223857
pharmgkbrs863223857
gwascentralrs863223857
openSNPrs863223857
23andMers863223857
23andMe allrs863223857
SNP Nexus

SNPshotrs863223857
SNPdbers863223857
MSV3drs863223857
GWAS Ctlgrs863223857
Max Magnitude0
ClinVar
Risk rs863223857(G;G)
Alt rs863223857(G;G)
Reference rs863223857(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFBR2
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.30713577A>G
CLNSRC
CLNACC RCV000200455.1,