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rs863223824

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223824(A;A)
Make rs863223824(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position99146498
GeneTGFBR1
is asnp
is mentioned by
dbSNPrs863223824
ebirs863223824
HLIrs863223824
Exacrs863223824
Varsomers863223824
Maprs863223824
PheGenIrs863223824
hapmaprs863223824
1000 genomesrs863223824
hgdprs863223824
ensemblrs863223824
gopubmedrs863223824
geneviewrs863223824
scholarrs863223824
googlers863223824
pharmgkbrs863223824
gwascentralrs863223824
openSNPrs863223824
23andMers863223824
23andMe allrs863223824
SNP Nexus

SNPshotrs863223824
SNPdbers863223824
MSV3drs863223824
GWAS Ctlgrs863223824
Max Magnitude0
ClinVar
Risk rs863223824(A;A)
Alt rs863223824(A;A)
Reference rs863223824(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene TGFBR1
CLNDBN not specified
Reversed 0
HGVS NC_000009.11:g.101908780G>A
CLNSRC
CLNACC RCV000196433.2,