Have questions? Visit https://www.reddit.com/r/SNPedia

rs281860306

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860306(A;G)
Make rs281860306(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position69816327
GeneFGF3
is asnp
is mentioned by
dbSNPrs281860306
ebirs281860306
HLIrs281860306
Exacrs281860306
Varsomers281860306
Maprs281860306
PheGenIrs281860306
hapmaprs281860306
1000 genomesrs281860306
hgdprs281860306
ensemblrs281860306
gopubmedrs281860306
geneviewrs281860306
scholarrs281860306
googlers281860306
pharmgkbrs281860306
gwascentralrs281860306
openSNPrs281860306
23andMers281860306
23andMe allrs281860306
SNP Nexus

SNPshotrs281860306
SNPdbers281860306
MSV3drs281860306
GWAS Ctlgrs281860306
Max Magnitude0
ClinVar
Risk rs281860306(G;G)
Alt rs281860306(G;G)
Reference rs281860306(A;A)
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.69631095T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000022693.27,