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rs771054241

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs771054241(A;T)
Make rs771054241(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position128395230
GeneFBN2
is asnp
is mentioned by
dbSNPrs771054241
ebirs771054241
HLIrs771054241
Exacrs771054241
Varsomers771054241
Maprs771054241
PheGenIrs771054241
hapmaprs771054241
1000 genomesrs771054241
hgdprs771054241
ensemblrs771054241
gopubmedrs771054241
geneviewrs771054241
scholarrs771054241
googlers771054241
pharmgkbrs771054241
gwascentralrs771054241
openSNPrs771054241
23andMers771054241
23andMe allrs771054241
SNP Nexus

SNPshotrs771054241
SNPdbers771054241
MSV3drs771054241
GWAS Ctlgrs771054241
Max Magnitude0
ClinVar
Risk rs771054241(T;T)
Alt rs771054241(T;T)
Reference rs771054241(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene FBN2
CLNDBN not specified
Reversed 0
HGVS NC_000005.9:g.127730923A>G
CLNSRC
CLNACC RCV000197199.2,