Have questions? Visit https://www.reddit.com/r/SNPedia

rs137854470

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854470(A;A)
Make rs137854470(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48487425
GeneFBN1
is asnp
is mentioned by
dbSNPrs137854470
ebirs137854470
HLIrs137854470
Exacrs137854470
Varsomers137854470
Maprs137854470
PheGenIrs137854470
hapmaprs137854470
1000 genomesrs137854470
hgdprs137854470
ensemblrs137854470
gopubmedrs137854470
geneviewrs137854470
scholarrs137854470
googlers137854470
pharmgkbrs137854470
gwascentralrs137854470
openSNPrs137854470
23andMers137854470
23andMe allrs137854470
SNP Nexus

SNPshotrs137854470
SNPdbers137854470
MSV3drs137854470
GWAS Ctlgrs137854470
Max Magnitude0
OMIM134797
Desc
Variant0025
Relatedalso
ClinVar
Risk rs137854470(A;A)
Alt rs137854470(A;A)
Reference rs137854470(G;G)
Significance Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48779622C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017890.27,