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rs727504411

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504411(A;A)
Make rs727504411(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position48487118
GeneFBN1
is asnp
is mentioned by
dbSNPrs727504411
ebirs727504411
HLIrs727504411
Exacrs727504411
Varsomers727504411
Maprs727504411
PheGenIrs727504411
hapmaprs727504411
1000 genomesrs727504411
hgdprs727504411
ensemblrs727504411
gopubmedrs727504411
geneviewrs727504411
scholarrs727504411
googlers727504411
pharmgkbrs727504411
gwascentralrs727504411
openSNPrs727504411
23andMers727504411
23andMe allrs727504411
SNP Nexus

SNPshotrs727504411
SNPdbers727504411
MSV3drs727504411
GWAS Ctlgrs727504411
Max Magnitude0
ClinVar
Risk rs727504411(A;A)
Alt rs727504411(A;A)
Reference rs727504411(C;C)
Significance Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48779315G>T
CLNSRC
CLNACC RCV000154599.1,