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rs373510719

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs373510719(G;G)
Make rs373510719(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48434711
GeneFBN1
is asnp
is mentioned by
dbSNPrs373510719
ebirs373510719
HLIrs373510719
Exacrs373510719
Varsomers373510719
Maprs373510719
PheGenIrs373510719
hapmaprs373510719
1000 genomesrs373510719
hgdprs373510719
ensemblrs373510719
gopubmedrs373510719
geneviewrs373510719
scholarrs373510719
googlers373510719
pharmgkbrs373510719
gwascentralrs373510719
openSNPrs373510719
23andMers373510719
23andMe allrs373510719
SNP Nexus

SNPshotrs373510719
SNPdbers373510719
MSV3drs373510719
GWAS Ctlgrs373510719
Max Magnitude0
ClinVar
Risk rs373510719(G;G)
Alt rs373510719(G;G)
Reference rs373510719(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.48726908T>G
CLNSRC
CLNACC RCV000181702.2,