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rs758366498

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs758366498(C;T)
Make rs758366498(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48488392
GeneFBN1
is asnp
is mentioned by
dbSNPrs758366498
ebirs758366498
HLIrs758366498
Exacrs758366498
Varsomers758366498
Maprs758366498
PheGenIrs758366498
hapmaprs758366498
1000 genomesrs758366498
hgdprs758366498
ensemblrs758366498
gopubmedrs758366498
geneviewrs758366498
scholarrs758366498
googlers758366498
pharmgkbrs758366498
gwascentralrs758366498
openSNPrs758366498
23andMers758366498
23andMe allrs758366498
SNP Nexus

SNPshotrs758366498
SNPdbers758366498
MSV3drs758366498
GWAS Ctlgrs758366498
Max Magnitude0
ClinVar
Risk rs758366498(T;T)
Alt rs758366498(T;T)
Reference rs758366498(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.48780589C>T
CLNSRC
CLNACC RCV000181481.2,