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rs1060501984

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060501984(C;T)
Make rs1060501984(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position30691426
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs1060501984
dbSNP (old)rs1060501984
ClinGenrs1060501984
ebirs1060501984
HLIrs1060501984
Exacrs1060501984
Gnomadrs1060501984
Varsomers1060501984
Maprs1060501984
PheGenIrs1060501984
Biobankrs1060501984
1000 genomesrs1060501984
hgdprs1060501984
ensemblrs1060501984
gopubmedrs1060501984
geneviewrs1060501984
scholarrs1060501984
googlers1060501984
pharmgkbrs1060501984
gwascentralrs1060501984
openSNPrs1060501984
23andMers1060501984
23andMe allrs1060501984
SNPshotrs1060501984
SNPdbers1060501984
MSV3drs1060501984
GWAS Ctlgrs1060501984
Max Magnitude0
ClinVar
Risk rs1060501984(T;T)
Alt rs1060501984(T;T)
Reference Rs1060501984(C;C)
Significance Probable-Pathogenic
Disease Thoracic aortic aneurysm and aortic dissection
Variation info
Gene TGFBR2
CLNDBN Thoracic aortic aneurysm and aortic dissection
Reversed 0
HGVS NC_000003.11:g.30732918C>T
CLNSRC
CLNACC RCV000456592.1,