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rs863223838

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223838(G;G)
Make rs863223838(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position30650418
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs863223838
ebirs863223838
HLIrs863223838
Exacrs863223838
Varsomers863223838
Maprs863223838
PheGenIrs863223838
hapmaprs863223838
1000 genomesrs863223838
hgdprs863223838
ensemblrs863223838
gopubmedrs863223838
geneviewrs863223838
scholarrs863223838
googlers863223838
pharmgkbrs863223838
gwascentralrs863223838
openSNPrs863223838
23andMers863223838
23andMe allrs863223838
SNP Nexus

SNPshotrs863223838
SNPdbers863223838
MSV3drs863223838
GWAS Ctlgrs863223838
Max Magnitude0
ClinVar
Risk rs863223838(G;G)
Alt rs863223838(G;G)
Reference rs863223838(T;T)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene TGFBR2
CLNDBN not specified
Reversed 0
HGVS NC_000003.11:g.30691910T>G
CLNSRC
CLNACC RCV000195915.2,