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rs34728766

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs34728766(A;A)
Make rs34728766(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position105143063
GeneJAG2
is asnp
is mentioned by
dbSNPrs34728766
ebirs34728766
HLIrs34728766
Exacrs34728766
Varsomers34728766
Maprs34728766
PheGenIrs34728766
hapmaprs34728766
1000 genomesrs34728766
hgdprs34728766
ensemblrs34728766
gopubmedrs34728766
geneviewrs34728766
scholarrs34728766
googlers34728766
pharmgkbrs34728766
gwascentralrs34728766
openSNPrs34728766
23andMers34728766
23andMe allrs34728766
SNP Nexus

SNPshotrs34728766
SNPdbers34728766
MSV3drs34728766
GWAS Ctlgrs34728766
GMAF0.005051
Max Magnitude0
Venter snp
Source plos
Gene JAG2
allele A
frequency
sift TOLERATED
HuRef 1103649153732
Disease Association May be associated with Usher syndrome type IA (USHA1A) which describes a congenital sensory deafness associated with retinitis pigmentosa and feeble-mindedness.