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rs763091520

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs763091520(G;T)
Make rs763091520(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48437912
GeneFBN1
is asnp
is mentioned by
dbSNPrs763091520
ebirs763091520
HLIrs763091520
Exacrs763091520
Varsomers763091520
Maprs763091520
PheGenIrs763091520
hapmaprs763091520
1000 genomesrs763091520
hgdprs763091520
ensemblrs763091520
gopubmedrs763091520
geneviewrs763091520
scholarrs763091520
googlers763091520
pharmgkbrs763091520
gwascentralrs763091520
openSNPrs763091520
23andMers763091520
23andMe allrs763091520
SNP Nexus

SNPshotrs763091520
SNPdbers763091520
MSV3drs763091520
GWAS Ctlgrs763091520
Max Magnitude0
ClinVar
Risk rs763091520(T;T)
Alt rs763091520(T;T)
Reference rs763091520(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.48730109G>A
CLNSRC
CLNACC RCV000181559.1,