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rs886038954

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs886038954(-;TG)
Make rs886038954(TG;TG)
ReferenceGRCh38.p7 38.3/149
Chromosome9
Position99147701
GeneTGFBR1
is asnp
is mentioned by
dbSNPrs886038954
dbSNP (classic)rs886038954
ClinGenrs886038954
ebirs886038954
HLIrs886038954
Exacrs886038954
Gnomadrs886038954
Varsomers886038954
LitVarrs886038954
Maprs886038954
PheGenIrs886038954
Biobankrs886038954
1000 genomesrs886038954
hgdprs886038954
ensemblrs886038954
geneviewrs886038954
scholarrs886038954
googlers886038954
pharmgkbrs886038954
gwascentralrs886038954
openSNPrs886038954
23andMers886038954
SNPshotrs886038954
SNPdbers886038954
MSV3drs886038954
GWAS Ctlgrs886038954
Max Magnitude0
ClinVar
Risk rs886038954(TG;TG)
Alt rs886038954(TG;TG)
Reference Rs886038954(-;-)
Significance 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.101909982_101909983dupTG
CLNSRC
CLNACC RCV000243082.1,