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rs112118237

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs112118237(C;T)
Make rs112118237(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position48420731
GeneFBN1
is asnp
is mentioned by
dbSNPrs112118237
ebirs112118237
HLIrs112118237
Exacrs112118237
Varsomers112118237
Maprs112118237
PheGenIrs112118237
hapmaprs112118237
1000 genomesrs112118237
hgdprs112118237
ensemblrs112118237
gopubmedrs112118237
geneviewrs112118237
scholarrs112118237
googlers112118237
pharmgkbrs112118237
gwascentralrs112118237
openSNPrs112118237
23andMers112118237
23andMe allrs112118237
SNP Nexus

SNPshotrs112118237
SNPdbers112118237
MSV3drs112118237
GWAS Ctlgrs112118237
Max Magnitude0
ClinVar
Risk rs112118237(T;T)
Alt rs112118237(T;T)
Reference rs112118237(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.48712928C>T
CLNSRC
CLNACC RCV000181614.2,