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rs886038919

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs886038919(A;G)
Make rs886038919(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome9
Position99138041
GeneTGFBR1
is asnp
is mentioned by
dbSNPrs886038919
dbSNP (classic)rs886038919
ClinGenrs886038919
ebirs886038919
HLIrs886038919
Exacrs886038919
Gnomadrs886038919
Varsomers886038919
LitVarrs886038919
Maprs886038919
PheGenIrs886038919
Biobankrs886038919
1000 genomesrs886038919
hgdprs886038919
ensemblrs886038919
geneviewrs886038919
scholarrs886038919
googlers886038919
pharmgkbrs886038919
gwascentralrs886038919
openSNPrs886038919
23andMers886038919
SNPshotrs886038919
SNPdbers886038919
MSV3drs886038919
GWAS Ctlgrs886038919
Max Magnitude0
ClinVar
Risk rs886038919(G;G)
Alt rs886038919(G;G)
Reference Rs886038919(A;A)
Significance Probable-Pathogenic
Disease Thoracic aortic aneurysm and aortic dissection
Variation info
Gene TGFBR1
CLNDBN Thoracic aortic aneurysm and aortic dissection
Reversed 0
HGVS NC_000009.11:g.101900323A>G
CLNSRC
CLNACC RCV000250999.1,