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rs761857514

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs761857514(C;T)
Make rs761857514(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48452676
GeneFBN1
is asnp
is mentioned by
dbSNPrs761857514
ebirs761857514
HLIrs761857514
Exacrs761857514
Varsomers761857514
Maprs761857514
PheGenIrs761857514
hapmaprs761857514
1000 genomesrs761857514
hgdprs761857514
ensemblrs761857514
gopubmedrs761857514
geneviewrs761857514
scholarrs761857514
googlers761857514
pharmgkbrs761857514
gwascentralrs761857514
openSNPrs761857514
23andMers761857514
23andMe allrs761857514
SNP Nexus

SNPshotrs761857514
SNPdbers761857514
MSV3drs761857514
GWAS Ctlgrs761857514
Max Magnitude0
ClinVar
Risk rs761857514(T;T)
Alt rs761857514(T;T)
Reference rs761857514(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.48744873C>T
CLNSRC
CLNACC RCV000181543.2,