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rs794728255

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728255(C;T)
Make rs794728255(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48432908
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728255
ebirs794728255
HLIrs794728255
Exacrs794728255
Varsomers794728255
Maprs794728255
PheGenIrs794728255
hapmaprs794728255
1000 genomesrs794728255
hgdprs794728255
ensemblrs794728255
gopubmedrs794728255
geneviewrs794728255
scholarrs794728255
googlers794728255
pharmgkbrs794728255
gwascentralrs794728255
openSNPrs794728255
23andMers794728255
23andMe allrs794728255
SNP Nexus

SNPshotrs794728255
SNPdbers794728255
MSV3drs794728255
GWAS Ctlgrs794728255
Max Magnitude0
ClinVar
Risk rs794728255(T;T)
Alt rs794728255(T;T)
Reference rs794728255(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48725105G>A
CLNSRC
CLNACC RCV000181576.1,