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rs747777955

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs747777955(C;C)
Make rs747777955(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48425392
GeneFBN1
is asnp
is mentioned by
dbSNPrs747777955
ebirs747777955
HLIrs747777955
Exacrs747777955
Varsomers747777955
Maprs747777955
PheGenIrs747777955
hapmaprs747777955
1000 genomesrs747777955
hgdprs747777955
ensemblrs747777955
gopubmedrs747777955
geneviewrs747777955
scholarrs747777955
googlers747777955
pharmgkbrs747777955
gwascentralrs747777955
openSNPrs747777955
23andMers747777955
23andMe allrs747777955
SNP Nexus

SNPshotrs747777955
SNPdbers747777955
MSV3drs747777955
GWAS Ctlgrs747777955
Max Magnitude0
ClinVar
Risk rs747777955(C;C)
Alt rs747777955(C;C)
Reference rs747777955(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.48717589T>C
CLNSRC
CLNACC RCV000181603.2,