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rs80356509

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80356509(A;A)
Make rs80356509(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position58097911
GeneFLNB
is asnp
is mentioned by
dbSNPrs80356509
ebirs80356509
HLIrs80356509
Exacrs80356509
Varsomers80356509
Maprs80356509
PheGenIrs80356509
hapmaprs80356509
1000 genomesrs80356509
hgdprs80356509
ensemblrs80356509
gopubmedrs80356509
geneviewrs80356509
scholarrs80356509
googlers80356509
pharmgkbrs80356509
gwascentralrs80356509
openSNPrs80356509
23andMers80356509
23andMe allrs80356509
SNP Nexus

SNPshotrs80356509
SNPdbers80356509
MSV3drs80356509
GWAS Ctlgrs80356509
Max Magnitude0
ClinVar
Risk rs80356509(A;A)
Alt rs80356509(A;A)
Reference rs80356509(G;G)
Significance Pathogenic
Disease Larsen syndrome
Variation info
Gene FLNB
CLNDBN Larsen syndrome, dominant type
Reversed 0
HGVS NC_000003.11:g.58083638G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000020441.2,