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rs727502791

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727502791(C;T)
Make rs727502791(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position8648141
GeneMFAP5
is asnp
is mentioned by
dbSNPrs727502791
ebirs727502791
HLIrs727502791
Exacrs727502791
Varsomers727502791
Maprs727502791
PheGenIrs727502791
hapmaprs727502791
1000 genomesrs727502791
hgdprs727502791
ensemblrs727502791
gopubmedrs727502791
geneviewrs727502791
scholarrs727502791
googlers727502791
pharmgkbrs727502791
gwascentralrs727502791
openSNPrs727502791
23andMers727502791
23andMe allrs727502791
SNP Nexus

SNPshotrs727502791
SNPdbers727502791
MSV3drs727502791
GWAS Ctlgrs727502791
Max Magnitude0
ClinVar
Risk rs727502791(T;T)
Alt rs727502791(T;T)
Reference rs727502791(C;C)
Significance Pathogenic
Disease Aortic aneurysm
Variation info
Gene MFAP5
CLNDBN Aortic aneurysm, familial thoracic 9
Reversed 1
HGVS NC_000012.11:g.8800737G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000149579.3,