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rs369294972

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs369294972(A;A)
Make rs369294972(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48421597
GeneFBN1
is asnp
is mentioned by
dbSNPrs369294972
ebirs369294972
HLIrs369294972
Exacrs369294972
Varsomers369294972
Maprs369294972
PheGenIrs369294972
hapmaprs369294972
1000 genomesrs369294972
hgdprs369294972
ensemblrs369294972
gopubmedrs369294972
geneviewrs369294972
scholarrs369294972
googlers369294972
pharmgkbrs369294972
gwascentralrs369294972
openSNPrs369294972
23andMers369294972
23andMe allrs369294972
SNP Nexus

SNPshotrs369294972
SNPdbers369294972
MSV3drs369294972
GWAS Ctlgrs369294972
Max Magnitude0
ClinVar
Risk rs369294972(A;A)
Alt rs369294972(A;A)
Reference rs369294972(G;G)
Significance Pathogenic
Disease Marfan syndrome not specified
Variation info
Gene FBN1
CLNDBN Marfan syndrome, incomplete not specified
Reversed 0
HGVS NC_000015.9:g.48713794G>A
CLNSRC
CLNACC RCV000148496.1, RCV000181611.2,