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rs534517447

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs534517447(A;A)
Make rs534517447(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position120956935
GeneGRIK4, LOC101929208
is asnp
is mentioned by
dbSNPrs534517447
ebirs534517447
HLIrs534517447
Exacrs534517447
Varsomers534517447
Maprs534517447
PheGenIrs534517447
hapmaprs534517447
1000 genomesrs534517447
hgdprs534517447
ensemblrs534517447
gopubmedrs534517447
geneviewrs534517447
scholarrs534517447
googlers534517447
pharmgkbrs534517447
gwascentralrs534517447
openSNPrs534517447
23andMers534517447
23andMe allrs534517447
SNP Nexus

SNPshotrs534517447
SNPdbers534517447
MSV3drs534517447
GWAS Ctlgrs534517447
Max Magnitude0
ClinVar
Risk rs534517447(A;A)
Alt rs534517447(A;A)
Reference rs534517447(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIK4 LOC101929208
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.120827644G>A
CLNSRC
CLNACC RCV000209911.1,