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rs281860300

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860300(A;G)
Make rs281860300(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position69818788
GeneFGF3
is asnp
is mentioned by
dbSNPrs281860300
ebirs281860300
HLIrs281860300
Exacrs281860300
Varsomers281860300
Maprs281860300
PheGenIrs281860300
hapmaprs281860300
1000 genomesrs281860300
hgdprs281860300
ensemblrs281860300
gopubmedrs281860300
geneviewrs281860300
scholarrs281860300
googlers281860300
pharmgkbrs281860300
gwascentralrs281860300
openSNPrs281860300
23andMers281860300
23andMe allrs281860300
SNP Nexus

SNPshotrs281860300
SNPdbers281860300
MSV3drs281860300
GWAS Ctlgrs281860300
Max Magnitude0
ClinVar
Risk rs281860300(G;G)
Alt rs281860300(G;G)
Reference rs281860300(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.69633556T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000022692.27,