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rs794728175

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728175(G;G)
Make rs794728175(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48508660
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728175
ebirs794728175
HLIrs794728175
Exacrs794728175
Varsomers794728175
Maprs794728175
PheGenIrs794728175
hapmaprs794728175
1000 genomesrs794728175
hgdprs794728175
ensemblrs794728175
gopubmedrs794728175
geneviewrs794728175
scholarrs794728175
googlers794728175
pharmgkbrs794728175
gwascentralrs794728175
openSNPrs794728175
23andMers794728175
23andMe allrs794728175
SNP Nexus

SNPshotrs794728175
SNPdbers794728175
MSV3drs794728175
GWAS Ctlgrs794728175
Max Magnitude0
ClinVar
Risk rs794728175(G;G)
Alt rs794728175(G;G)
Reference Rs794728175(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48800857A>C
CLNSRC
CLNACC RCV000181441.2,