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rs281860304

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860304(-;-)
Make rs281860304(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position69810631
GeneFGF3
is asnp
is mentioned by
dbSNPrs281860304
ebirs281860304
HLIrs281860304
Exacrs281860304
Varsomers281860304
Maprs281860304
PheGenIrs281860304
hapmaprs281860304
1000 genomesrs281860304
hgdprs281860304
ensemblrs281860304
gopubmedrs281860304
geneviewrs281860304
scholarrs281860304
googlers281860304
pharmgkbrs281860304
gwascentralrs281860304
openSNPrs281860304
23andMers281860304
23andMe allrs281860304
SNP Nexus

SNPshotrs281860304
SNPdbers281860304
MSV3drs281860304
GWAS Ctlgrs281860304
Max Magnitude0
ClinVar
Risk rs281860304(;)
Alt rs281860304(;)
Reference rs281860304(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.69625399delG
CLNSRC ClinVar GeneReviews
CLNACC RCV000031940.1,