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rs863223853

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223853(G;T)
Make rs863223853(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position30691421
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs863223853
ebirs863223853
HLIrs863223853
Exacrs863223853
Varsomers863223853
Maprs863223853
PheGenIrs863223853
hapmaprs863223853
1000 genomesrs863223853
hgdprs863223853
ensemblrs863223853
gopubmedrs863223853
geneviewrs863223853
scholarrs863223853
googlers863223853
pharmgkbrs863223853
gwascentralrs863223853
openSNPrs863223853
23andMers863223853
23andMe allrs863223853
SNP Nexus

SNPshotrs863223853
SNPdbers863223853
MSV3drs863223853
GWAS Ctlgrs863223853
Max Magnitude0
ClinVar
Risk rs863223853(T;T)
Alt rs863223853(T;T)
Reference rs863223853(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TGFBR2
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.30732913G>T
CLNSRC
CLNACC RCV000195860.1,