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rs794728178

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728178(A;T)
Make rs794728178(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48505096
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728178
ebirs794728178
HLIrs794728178
Exacrs794728178
Varsomers794728178
Maprs794728178
PheGenIrs794728178
hapmaprs794728178
1000 genomesrs794728178
hgdprs794728178
ensemblrs794728178
gopubmedrs794728178
geneviewrs794728178
scholarrs794728178
googlers794728178
pharmgkbrs794728178
gwascentralrs794728178
openSNPrs794728178
23andMers794728178
23andMe allrs794728178
SNP Nexus

SNPshotrs794728178
SNPdbers794728178
MSV3drs794728178
GWAS Ctlgrs794728178
Max Magnitude0
ClinVar
Risk rs794728178(T;T)
Alt rs794728178(T;T)
Reference rs794728178(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48797293T>A
CLNSRC
CLNACC RCV000181446.1,