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rs863223819

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223819(A;G)
Make rs863223819(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position99138081
GeneTGFBR1
is asnp
is mentioned by
dbSNPrs863223819
ebirs863223819
HLIrs863223819
Exacrs863223819
Varsomers863223819
Maprs863223819
PheGenIrs863223819
hapmaprs863223819
1000 genomesrs863223819
hgdprs863223819
ensemblrs863223819
gopubmedrs863223819
geneviewrs863223819
scholarrs863223819
googlers863223819
pharmgkbrs863223819
gwascentralrs863223819
openSNPrs863223819
23andMers863223819
23andMe allrs863223819
SNP Nexus

SNPshotrs863223819
SNPdbers863223819
MSV3drs863223819
GWAS Ctlgrs863223819
Max Magnitude0
ClinVar
Risk rs863223819(G;G)
Alt rs863223819(G;G)
Reference rs863223819(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TGFBR1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.101900363A>G
CLNSRC
CLNACC RCV000197559.1,