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rs863223845

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223845(G;T)
Make rs863223845(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position30672372
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs863223845
ebirs863223845
HLIrs863223845
Exacrs863223845
Varsomers863223845
Maprs863223845
PheGenIrs863223845
hapmaprs863223845
1000 genomesrs863223845
hgdprs863223845
ensemblrs863223845
gopubmedrs863223845
geneviewrs863223845
scholarrs863223845
googlers863223845
pharmgkbrs863223845
gwascentralrs863223845
openSNPrs863223845
23andMers863223845
23andMe allrs863223845
SNP Nexus

SNPshotrs863223845
SNPdbers863223845
MSV3drs863223845
GWAS Ctlgrs863223845
Max Magnitude0
ClinVar
Risk rs863223845(T;T)
Alt rs863223845(T;T)
Reference rs863223845(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFBR2
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.30713864G>T
CLNSRC
CLNACC RCV000198267.1,