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rs863223830

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTC;CTC) 0 common in clinvar
Make rs863223830(-;-)
Make rs863223830(-;CTC)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position99137989
GeneTGFBR1
is asnp
is mentioned by
dbSNPrs863223830
dbSNP (old)rs863223830
ClinGenrs863223830
ebirs863223830
HLIrs863223830
Exacrs863223830
Gnomadrs863223830
Varsomers863223830
Maprs863223830
PheGenIrs863223830
Biobankrs863223830
1000 genomesrs863223830
hgdprs863223830
ensemblrs863223830
gopubmedrs863223830
geneviewrs863223830
scholarrs863223830
googlers863223830
pharmgkbrs863223830
gwascentralrs863223830
openSNPrs863223830
23andMers863223830
23andMe allrs863223830
SNP Nexus

SNPshotrs863223830
SNPdbers863223830
MSV3drs863223830
GWAS Ctlgrs863223830
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs863223830(CTC;CTC)
Significance Pathogenic
Disease not provided
Variation info
Gene TGFBR1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.101900271_101900273delCTC
CLNSRC
CLNACC RCV000198926.1,