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rs863223849

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223849(A;A)
Make rs863223849(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position30674126
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs863223849
ebirs863223849
HLIrs863223849
Exacrs863223849
Varsomers863223849
Maprs863223849
PheGenIrs863223849
hapmaprs863223849
1000 genomesrs863223849
hgdprs863223849
ensemblrs863223849
gopubmedrs863223849
geneviewrs863223849
scholarrs863223849
googlers863223849
pharmgkbrs863223849
gwascentralrs863223849
openSNPrs863223849
23andMers863223849
23andMe allrs863223849
SNP Nexus

SNPshotrs863223849
SNPdbers863223849
MSV3drs863223849
GWAS Ctlgrs863223849
Max Magnitude0
ClinVar
Risk rs863223849(A;A)
Alt rs863223849(A;A)
Reference rs863223849(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TGFBR2
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.30715618G>A
CLNSRC
CLNACC RCV000197140.1,