Have questions? Visit https://www.reddit.com/r/SNPedia

rs863223818

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223818(A;A)
Make rs863223818(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position99142704
GeneTGFBR1
is asnp
is mentioned by
dbSNPrs863223818
ebirs863223818
HLIrs863223818
Exacrs863223818
Varsomers863223818
Maprs863223818
PheGenIrs863223818
hapmaprs863223818
1000 genomesrs863223818
hgdprs863223818
ensemblrs863223818
gopubmedrs863223818
geneviewrs863223818
scholarrs863223818
googlers863223818
pharmgkbrs863223818
gwascentralrs863223818
openSNPrs863223818
23andMers863223818
23andMe allrs863223818
SNP Nexus

SNPshotrs863223818
SNPdbers863223818
MSV3drs863223818
GWAS Ctlgrs863223818
Max Magnitude0
ClinVar
Risk rs863223818(A;A)
Alt rs863223818(A;A)
Reference rs863223818(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TGFBR1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.101904986G>A
CLNSRC
CLNACC RCV000196022.2,