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rs146469379

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs146469379(A;A)
Make rs146469379(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position48415560
GeneFBN1
is asnp
is mentioned by
dbSNPrs146469379
dbSNP (old)rs146469379
ClinGenrs146469379
ebirs146469379
HLIrs146469379
Exacrs146469379
Gnomadrs146469379
Varsomers146469379
Maprs146469379
PheGenIrs146469379
Biobankrs146469379
1000 genomesrs146469379
hgdprs146469379
ensemblrs146469379
gopubmedrs146469379
geneviewrs146469379
scholarrs146469379
googlers146469379
pharmgkbrs146469379
gwascentralrs146469379
openSNPrs146469379
23andMers146469379
23andMe allrs146469379
SNPshotrs146469379
SNPdbers146469379
MSV3drs146469379
GWAS Ctlgrs146469379
Max Magnitude0
ClinVar
Risk rs146469379(A;A)
Alt rs146469379(A;A)
Reference Rs146469379(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.48707757G>A
CLNSRC
CLNACC RCV000483455.1,