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rs863223854

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223854(A;A)
Make rs863223854(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position30691459
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs863223854
ebirs863223854
HLIrs863223854
Exacrs863223854
Varsomers863223854
Maprs863223854
PheGenIrs863223854
hapmaprs863223854
1000 genomesrs863223854
hgdprs863223854
ensemblrs863223854
gopubmedrs863223854
geneviewrs863223854
scholarrs863223854
googlers863223854
pharmgkbrs863223854
gwascentralrs863223854
openSNPrs863223854
23andMers863223854
23andMe allrs863223854
SNP Nexus

SNPshotrs863223854
SNPdbers863223854
MSV3drs863223854
GWAS Ctlgrs863223854
Max Magnitude0
ClinVar
Risk rs863223854(A;A)
Alt rs863223854(A;A)
Reference rs863223854(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TGFBR2
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.30732951G>A
CLNSRC
CLNACC RCV000198083.1,