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rs281860307

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs281860307(-;-)
Make rs281860307(-;TG)
ReferenceGRCh38 38.1/141
Chromosome11
Position69810567
GeneFGF3
is asnp
is mentioned by
dbSNPrs281860307
ebirs281860307
HLIrs281860307
Exacrs281860307
Varsomers281860307
Maprs281860307
PheGenIrs281860307
hapmaprs281860307
1000 genomesrs281860307
hgdprs281860307
ensemblrs281860307
gopubmedrs281860307
geneviewrs281860307
scholarrs281860307
googlers281860307
pharmgkbrs281860307
gwascentralrs281860307
openSNPrs281860307
23andMers281860307
23andMe allrs281860307
SNP Nexus

SNPshotrs281860307
SNPdbers281860307
MSV3drs281860307
GWAS Ctlgrs281860307
Max Magnitude0
ClinVar
Risk rs281860307(;)
Alt rs281860307(;)
Reference rs281860307(TG;TG)
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.69625335_69625336delCA
CLNSRC OMIM Allelic Variant
CLNACC RCV000022694.28,