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rs863223844

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223844(A;A)
Make rs863223844(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position30672328
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs863223844
ebirs863223844
HLIrs863223844
Exacrs863223844
Varsomers863223844
Maprs863223844
PheGenIrs863223844
hapmaprs863223844
1000 genomesrs863223844
hgdprs863223844
ensemblrs863223844
gopubmedrs863223844
geneviewrs863223844
scholarrs863223844
googlers863223844
pharmgkbrs863223844
gwascentralrs863223844
openSNPrs863223844
23andMers863223844
23andMe allrs863223844
SNP Nexus

SNPshotrs863223844
SNPdbers863223844
MSV3drs863223844
GWAS Ctlgrs863223844
Max Magnitude0
ClinVar
Risk rs863223844(A;A)
Alt rs863223844(A;A)
Reference rs863223844(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFBR2
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.30713820G>A
CLNSRC
CLNACC RCV000198413.1,