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rs39395

From SNPedia

Orientationplus
Stabilizedplus
Make rs39395(A;A)
Make rs39395(A;G)
Make rs39395(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position103849282
GeneRELN
is asnp
is mentioned by
dbSNPrs39395
ebirs39395
HLIrs39395
Exacrs39395
Varsomers39395
Maprs39395
PheGenIrs39395
hapmaprs39395
1000 genomesrs39395
hgdprs39395
ensemblrs39395
gopubmedrs39395
geneviewrs39395
scholarrs39395
googlers39395
pharmgkbrs39395
gwascentralrs39395
openSNPrs39395
23andMers39395
23andMe allrs39395
SNP Nexus

SNPshotrs39395
SNPdbers39395
MSV3drs39395
GWAS Ctlgrs39395
GMAF0.4624
Max Magnitude
? (A;A) (A;G) (G;G) 28
OMIM166800
DescOTOSCLEROSIS; OTSC1
Variant
Relatedalso
[PMID 19230858OA-icon.png] A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.