Have questions? Visit https://www.reddit.com/r/SNPedia

rs746167150

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs746167150(C;T)
Make rs746167150(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48437054
GeneFBN1
is asnp
is mentioned by
dbSNPrs746167150
ClinGenrs746167150
ebirs746167150
HLIrs746167150
Exacrs746167150
Varsomers746167150
Maprs746167150
PheGenIrs746167150
hapmaprs746167150
1000 genomesrs746167150
hgdprs746167150
ensemblrs746167150
gopubmedrs746167150
geneviewrs746167150
scholarrs746167150
googlers746167150
pharmgkbrs746167150
gwascentralrs746167150
openSNPrs746167150
23andMers746167150
23andMe allrs746167150
SNP Nexus

SNPshotrs746167150
SNPdbers746167150
MSV3drs746167150
GWAS Ctlgrs746167150
Max Magnitude0
ClinVar
Risk rs746167150(T;T)
Alt rs746167150(T;T)
Reference Rs746167150(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.48729251C>T
CLNSRC
CLNACC RCV000181564.2,