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rs113422242

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs113422242(C;T)
Make rs113422242(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position48510065
GeneFBN1
is asnp
is mentioned by
dbSNPrs113422242
ebirs113422242
HLIrs113422242
Exacrs113422242
Varsomers113422242
Maprs113422242
PheGenIrs113422242
hapmaprs113422242
1000 genomesrs113422242
hgdprs113422242
ensemblrs113422242
gopubmedrs113422242
geneviewrs113422242
scholarrs113422242
googlers113422242
pharmgkbrs113422242
gwascentralrs113422242
openSNPrs113422242
23andMers113422242
23andMe allrs113422242
SNP Nexus

SNPshotrs113422242
SNPdbers113422242
MSV3drs113422242
GWAS Ctlgrs113422242
Max Magnitude0
ClinVar
Risk rs113422242(T;T)
Alt rs113422242(T;T)
Reference rs113422242(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48802262G>A
CLNSRC
CLNACC RCV000181438.2,