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rs281860301

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860301(A;A)
Make rs281860301(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position69818784
GeneFGF3
is asnp
is mentioned by
dbSNPrs281860301
ebirs281860301
HLIrs281860301
Exacrs281860301
Varsomers281860301
Maprs281860301
PheGenIrs281860301
hapmaprs281860301
1000 genomesrs281860301
hgdprs281860301
ensemblrs281860301
gopubmedrs281860301
geneviewrs281860301
scholarrs281860301
googlers281860301
pharmgkbrs281860301
gwascentralrs281860301
openSNPrs281860301
23andMers281860301
23andMe allrs281860301
SNP Nexus

SNPshotrs281860301
SNPdbers281860301
MSV3drs281860301
GWAS Ctlgrs281860301
Max Magnitude0
ClinVar
Risk rs281860301(A;A)
Alt rs281860301(A;A)
Reference rs281860301(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.69633552G>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000031938.1,