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rs863224935

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224935(G;G)
Make rs863224935(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position30688395
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs863224935
ebirs863224935
HLIrs863224935
Exacrs863224935
Varsomers863224935
Maprs863224935
PheGenIrs863224935
hapmaprs863224935
1000 genomesrs863224935
hgdprs863224935
ensemblrs863224935
gopubmedrs863224935
geneviewrs863224935
scholarrs863224935
googlers863224935
pharmgkbrs863224935
gwascentralrs863224935
openSNPrs863224935
23andMers863224935
23andMe allrs863224935
SNP Nexus

SNPshotrs863224935
SNPdbers863224935
MSV3drs863224935
GWAS Ctlgrs863224935
Max Magnitude0
ClinVar
Risk rs863224935(G;G)
Alt rs863224935(G;G)
Reference rs863224935(T;T)
Significance Probable-Pathogenic
Disease Loeys-Dietz syndrome 2
Variation info
Gene TGFBR2
CLNDBN Loeys-Dietz syndrome 2
Reversed 0
HGVS NC_000003.11:g.30729887T>G
CLNSRC
CLNACC RCV000197170.1,