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rs778181932

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs778181932(C;T)
Make rs778181932(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48488431
GeneFBN1
is asnp
is mentioned by
dbSNPrs778181932
ebirs778181932
HLIrs778181932
Exacrs778181932
Varsomers778181932
Maprs778181932
PheGenIrs778181932
hapmaprs778181932
1000 genomesrs778181932
hgdprs778181932
ensemblrs778181932
gopubmedrs778181932
geneviewrs778181932
scholarrs778181932
googlers778181932
pharmgkbrs778181932
gwascentralrs778181932
openSNPrs778181932
23andMers778181932
23andMe allrs778181932
SNP Nexus

SNPshotrs778181932
SNPdbers778181932
MSV3drs778181932
GWAS Ctlgrs778181932
Max Magnitude0
ClinVar
Risk rs778181932(T;T)
Alt rs778181932(T;T)
Reference rs778181932(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.48780628C>A
CLNSRC
CLNACC RCV000181479.1,