Have questions? Visit https://www.reddit.com/r/SNPedia

rs770443276

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs770443276(C;T)
Make rs770443276(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48428426
GeneFBN1
is asnp
is mentioned by
dbSNPrs770443276
ebirs770443276
HLIrs770443276
Exacrs770443276
Varsomers770443276
Maprs770443276
PheGenIrs770443276
hapmaprs770443276
1000 genomesrs770443276
hgdprs770443276
ensemblrs770443276
gopubmedrs770443276
geneviewrs770443276
scholarrs770443276
googlers770443276
pharmgkbrs770443276
gwascentralrs770443276
openSNPrs770443276
23andMers770443276
23andMe allrs770443276
SNP Nexus

SNPshotrs770443276
SNPdbers770443276
MSV3drs770443276
GWAS Ctlgrs770443276
Max Magnitude0
ClinVar
Risk rs770443276(T;T)
Alt rs770443276(T;T)
Reference rs770443276(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.48720623C>T
CLNSRC
CLNACC RCV000181583.1,