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rs80356499

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80356499(C;T)
Make rs80356499(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position58078777
GeneFLNB
is asnp
is mentioned by
dbSNPrs80356499
ebirs80356499
HLIrs80356499
Exacrs80356499
Varsomers80356499
Maprs80356499
PheGenIrs80356499
hapmaprs80356499
1000 genomesrs80356499
hgdprs80356499
ensemblrs80356499
gopubmedrs80356499
geneviewrs80356499
scholarrs80356499
googlers80356499
pharmgkbrs80356499
gwascentralrs80356499
openSNPrs80356499
23andMers80356499
23andMe allrs80356499
SNP Nexus

SNPshotrs80356499
SNPdbers80356499
MSV3drs80356499
GWAS Ctlgrs80356499
Max Magnitude0
ClinVar
Risk rs80356499(T;T)
Alt rs80356499(T;T)
Reference rs80356499(C;C)
Significance Pathogenic
Disease Atelosteogenesis type 3
Variation info
Gene FLNB
CLNDBN Atelosteogenesis type 3
Reversed 0
HGVS NC_000003.11:g.58064504C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000020456.2,