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rs281860303

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860303(C;T)
Make rs281860303(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position69816361
GeneFGF3
is asnp
is mentioned by
dbSNPrs281860303
ebirs281860303
HLIrs281860303
Exacrs281860303
Varsomers281860303
Maprs281860303
PheGenIrs281860303
hapmaprs281860303
1000 genomesrs281860303
hgdprs281860303
ensemblrs281860303
gopubmedrs281860303
geneviewrs281860303
scholarrs281860303
googlers281860303
pharmgkbrs281860303
gwascentralrs281860303
openSNPrs281860303
23andMers281860303
23andMe allrs281860303
SNP Nexus

SNPshotrs281860303
SNPdbers281860303
MSV3drs281860303
GWAS Ctlgrs281860303
Max Magnitude0
ClinVar
Risk rs281860303(T;T)
Alt rs281860303(T;T)
Reference rs281860303(C;C)
Significance Pathogenic
Disease Deafness with labyrinthine aplasia microtia and microdontia (LAMM)
Variation info
Gene FGF3
CLNDBN Deafness with labyrinthine aplasia microtia and microdontia (LAMM)
Reversed 1
HGVS NC_000011.9:g.69631129G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000031939.1,