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rs39335

From SNPedia

Orientationminus
Stabilizedminus
Make rs39335(A;A)
Make rs39335(A;G)
Make rs39335(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position103813122
GeneRELN
is asnp
is mentioned by
dbSNPrs39335
ebirs39335
HLIrs39335
Exacrs39335
Varsomers39335
Maprs39335
PheGenIrs39335
hapmaprs39335
1000 genomesrs39335
hgdprs39335
ensemblrs39335
gopubmedrs39335
geneviewrs39335
scholarrs39335
googlers39335
pharmgkbrs39335
gwascentralrs39335
openSNPrs39335
23andMers39335
23andMe allrs39335
SNP Nexus

SNPshotrs39335
SNPdbers39335
MSV3drs39335
GWAS Ctlgrs39335
GMAF0.1676
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 24227897OA-icon.png] The rs39335 polymorphism of the RELN gene is not associated with otosclerosis in a southern Italian population


[PMID 19230858OA-icon.png] A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.