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rs869025537

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025537(A;A)
Make rs869025537(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position30672235
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs869025537
ebirs869025537
HLIrs869025537
Exacrs869025537
Varsomers869025537
Maprs869025537
PheGenIrs869025537
hapmaprs869025537
1000 genomesrs869025537
hgdprs869025537
ensemblrs869025537
gopubmedrs869025537
geneviewrs869025537
scholarrs869025537
googlers869025537
pharmgkbrs869025537
gwascentralrs869025537
openSNPrs869025537
23andMers869025537
23andMe allrs869025537
SNP Nexus

SNPshotrs869025537
SNPdbers869025537
MSV3drs869025537
GWAS Ctlgrs869025537
Max Magnitude0
ClinVar
Risk rs869025537(A;A)
Alt rs869025537(A;A)
Reference rs869025537(G;G)
Significance Probable-Pathogenic
Disease Loeys-Dietz syndrome
Variation info
Gene TGFBR2
CLNDBN Loeys-Dietz syndrome
Reversed 0
HGVS NC_000003.11:g.30713727G>A
CLNSRC
CLNACC RCV000208228.1,