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rs148076256

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs148076256(C;C)
Make rs148076256(C;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48489907
GeneFBN1
is asnp
is mentioned by
dbSNPrs148076256
ebirs148076256
HLIrs148076256
Exacrs148076256
Varsomers148076256
Maprs148076256
PheGenIrs148076256
hapmaprs148076256
1000 genomesrs148076256
hgdprs148076256
ensemblrs148076256
gopubmedrs148076256
geneviewrs148076256
scholarrs148076256
googlers148076256
pharmgkbrs148076256
gwascentralrs148076256
openSNPrs148076256
23andMers148076256
23andMe allrs148076256
SNP Nexus

SNPshotrs148076256
SNPdbers148076256
MSV3drs148076256
GWAS Ctlgrs148076256
Max Magnitude0
ClinVar
Risk rs148076256(C;C)
Alt rs148076256(C;C)
Reference rs148076256(G;G)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 0
HGVS NC_000015.9:g.48782104G>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029721.1,