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rs730880108

From SNPedia

Orientationminus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs730880108(-;-)
Make rs730880108(-;TA)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position48610753
GeneFBN1
is asnp
is mentioned by
dbSNPrs730880108
ebirs730880108
HLIrs730880108
Exacrs730880108
Varsomers730880108
Maprs730880108
PheGenIrs730880108
hapmaprs730880108
1000 genomesrs730880108
hgdprs730880108
ensemblrs730880108
gopubmedrs730880108
geneviewrs730880108
scholarrs730880108
googlers730880108
pharmgkbrs730880108
gwascentralrs730880108
openSNPrs730880108
23andMers730880108
23andMe allrs730880108
SNP Nexus

SNPshotrs730880108
SNPdbers730880108
MSV3drs730880108
GWAS Ctlgrs730880108
Max Magnitude0
ClinVar
Risk rs730880108(;)
Alt rs730880108(;)
Reference rs730880108(TA;TA)
Significance Probable-Pathogenic
Disease Marfan syndrome
Variation info
Gene FBN1
CLNDBN Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48902950_48902951delTA
CLNSRC
CLNACC RCV000157235.1,