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rs80356504

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80356504(A;A)
Make rs80356504(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position58077255
GeneFLNB
is asnp
is mentioned by
dbSNPrs80356504
ebirs80356504
HLIrs80356504
Exacrs80356504
Varsomers80356504
Maprs80356504
PheGenIrs80356504
hapmaprs80356504
1000 genomesrs80356504
hgdprs80356504
ensemblrs80356504
gopubmedrs80356504
geneviewrs80356504
scholarrs80356504
googlers80356504
pharmgkbrs80356504
gwascentralrs80356504
openSNPrs80356504
23andMers80356504
23andMe allrs80356504
SNP Nexus

SNPshotrs80356504
SNPdbers80356504
MSV3drs80356504
GWAS Ctlgrs80356504
Max Magnitude0
ClinVar
Risk rs80356504(A;A)
Alt rs80356504(A;A)
Reference rs80356504(G;G)
Significance Pathogenic
Disease FLNB-Related Disorders
Variation info
Gene FLNB
CLNDBN FLNB-Related Disorders
Reversed 0
HGVS NC_000003.11:g.58062982G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000032212.2,