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rs10489678

From SNPedia

Orientationplus
Stabilizedplus
Make rs10489678(A;A)
Make rs10489678(A;G)
Make rs10489678(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position157699878
GeneFCRL3
is asnp
is mentioned by
dbSNPrs10489678
ebirs10489678
HLIrs10489678
Exacrs10489678
Varsomers10489678
Maprs10489678
PheGenIrs10489678
hapmaprs10489678
1000 genomesrs10489678
hgdprs10489678
ensemblrs10489678
gopubmedrs10489678
geneviewrs10489678
scholarrs10489678
googlers10489678
pharmgkbrs10489678
gwascentralrs10489678
openSNPrs10489678
23andMers10489678
23andMe allrs10489678
SNP Nexus

SNPshotrs10489678
SNPdbers10489678
MSV3drs10489678
GWAS Ctlgrs10489678
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 26051414] FCRL3 gene polymorphisms confer risk for sudden sensorineural hearing loss in a Chinese Han Population