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rs281860305

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860305(-;-)
Make rs281860305(-;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position69810409
GeneFGF3
is asnp
is mentioned by
dbSNPrs281860305
ebirs281860305
HLIrs281860305
Exacrs281860305
Varsomers281860305
Maprs281860305
PheGenIrs281860305
hapmaprs281860305
1000 genomesrs281860305
hgdprs281860305
ensemblrs281860305
gopubmedrs281860305
geneviewrs281860305
scholarrs281860305
googlers281860305
pharmgkbrs281860305
gwascentralrs281860305
openSNPrs281860305
23andMers281860305
23andMe allrs281860305
SNP Nexus

SNPshotrs281860305
SNPdbers281860305
MSV3drs281860305
GWAS Ctlgrs281860305
Max Magnitude0
ClinVar
Risk rs281860305(;)
Alt rs281860305(;)
Reference rs281860305(G;G)
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.69625177delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000014851.26,