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rs140630

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs140630(C;T)
Make rs140630(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48465580
GeneFBN1
is asnp
is mentioned by
dbSNPrs140630
ebirs140630
HLIrs140630
Exacrs140630
Varsomers140630
Maprs140630
PheGenIrs140630
hapmaprs140630
1000 genomesrs140630
hgdprs140630
ensemblrs140630
gopubmedrs140630
geneviewrs140630
scholarrs140630
googlers140630
pharmgkbrs140630
gwascentralrs140630
openSNPrs140630
23andMers140630
23andMe allrs140630
SNP Nexus

SNPshotrs140630
SNPdbers140630
MSV3drs140630
GWAS Ctlgrs140630
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs140630(T;T)
Alt rs140630(T;T)
Reference rs140630(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48757777G>A
CLNSRC
CLNACC RCV000181693.1,