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rs869312699

From SNPedia

Orientationplus
Geno Mag Summary
(CTGGCGCAGGAGGCC;CTGGCGCAGGAGGCC) 0 common in clinvar
Make rs869312699(CTGGCGCAGGAGGCC;GCT)
Make rs869312699(GCT;GCT)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position120986102
GeneGRIK4
is asnp
is mentioned by
dbSNPrs869312699
ebirs869312699
HLIrs869312699
Exacrs869312699
Varsomers869312699
Maprs869312699
PheGenIrs869312699
hapmaprs869312699
1000 genomesrs869312699
hgdprs869312699
ensemblrs869312699
gopubmedrs869312699
geneviewrs869312699
scholarrs869312699
googlers869312699
pharmgkbrs869312699
gwascentralrs869312699
openSNPrs869312699
23andMers869312699
23andMe allrs869312699
SNP Nexus

SNPshotrs869312699
SNPdbers869312699
MSV3drs869312699
GWAS Ctlgrs869312699
Max Magnitude0
ClinVar
Risk rs869312699(GCT;GCT)
Alt rs869312699(GCT;GCT)
Reference rs869312699(CTGGCGCAGGAGGCC;CTGGCGCAGGAGGCC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIK4
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.120856811_120856825delCTGGCGCAGGAGGCCinsGCT
CLNSRC
CLNACC RCV000209841.1,