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rs2286194

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs2286194(A;A)
Make rs2286194(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position81726133
GeneHGF
is asnp
is mentioned by
dbSNPrs2286194
ebirs2286194
HLIrs2286194
Exacrs2286194
Varsomers2286194
Maprs2286194
PheGenIrs2286194
hapmaprs2286194
1000 genomesrs2286194
hgdprs2286194
ensemblrs2286194
gopubmedrs2286194
geneviewrs2286194
scholarrs2286194
googlers2286194
pharmgkbrs2286194
gwascentralrs2286194
openSNPrs2286194
23andMers2286194
23andMe allrs2286194
SNP Nexus

SNPshotrs2286194
SNPdbers2286194
MSV3drs2286194
GWAS Ctlgrs2286194
GMAF0.1979
Max Magnitude0
? (A;A) (A;T) (T;T) 28
[PMID 19471602OA-icon.png] Hepatocyte growth factor and myopia: Genetic association analyses in a caucasian population

[PMID 19576567OA-icon.png] Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.