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rs80356505

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80356505(A;A)
Make rs80356505(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position58136142
GeneFLNB
is asnp
is mentioned by
dbSNPrs80356505
ebirs80356505
HLIrs80356505
Exacrs80356505
Varsomers80356505
Maprs80356505
PheGenIrs80356505
hapmaprs80356505
1000 genomesrs80356505
hgdprs80356505
ensemblrs80356505
gopubmedrs80356505
geneviewrs80356505
scholarrs80356505
googlers80356505
pharmgkbrs80356505
gwascentralrs80356505
openSNPrs80356505
23andMers80356505
23andMe allrs80356505
SNP Nexus

SNPshotrs80356505
SNPdbers80356505
MSV3drs80356505
GWAS Ctlgrs80356505
Max Magnitude0
ClinVar
Risk rs80356505(A;A)
Alt rs80356505(A;A)
Reference rs80356505(G;G)
Significance Pathogenic
Disease FLNB-Related Disorders
Variation info
Gene FLNB
CLNDBN FLNB-Related Disorders
Reversed 0
HGVS NC_000003.11:g.58121869G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000032211.2,