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rs794728188

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728188(C;T)
Make rs794728188(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48497332
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728188
ebirs794728188
HLIrs794728188
Exacrs794728188
Varsomers794728188
Maprs794728188
PheGenIrs794728188
hapmaprs794728188
1000 genomesrs794728188
hgdprs794728188
ensemblrs794728188
gopubmedrs794728188
geneviewrs794728188
scholarrs794728188
googlers794728188
pharmgkbrs794728188
gwascentralrs794728188
openSNPrs794728188
23andMers794728188
23andMe allrs794728188
SNP Nexus

SNPshotrs794728188
SNPdbers794728188
MSV3drs794728188
GWAS Ctlgrs794728188
Max Magnitude0
ClinVar
Risk rs794728188(T;T)
Alt rs794728188(T;T)
Reference rs794728188(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48789529G>A
CLNSRC
CLNACC RCV000181457.2,