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rs869312699

From SNPedia

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,