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rs80356510

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80356510(A;A)
Make rs80356510(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position58097918
GeneFLNB
is asnp
is mentioned by
dbSNPrs80356510
ebirs80356510
HLIrs80356510
Exacrs80356510
Varsomers80356510
Maprs80356510
PheGenIrs80356510
hapmaprs80356510
1000 genomesrs80356510
hgdprs80356510
ensemblrs80356510
gopubmedrs80356510
geneviewrs80356510
scholarrs80356510
googlers80356510
pharmgkbrs80356510
gwascentralrs80356510
openSNPrs80356510
23andMers80356510
23andMe allrs80356510
SNP Nexus

SNPshotrs80356510
SNPdbers80356510
MSV3drs80356510
GWAS Ctlgrs80356510
Max Magnitude0
ClinVar
Risk rs80356510(A;A)
Alt rs80356510(A;A)
Reference rs80356510(G;G)
Significance Pathogenic
Disease Larsen syndrome
Variation info
Gene FLNB
CLNDBN Larsen syndrome, dominant type
Reversed 0
HGVS NC_000003.11:g.58083645G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000020442.2,