rs869312699

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(CTGGCGCAGGAGGCC;CTGGCGCAGGAGGCC)	0	common in clinvar

Make rs869312699(CTGGCGCAGGAGGCC;GCT)

Make rs869312699(GCT;GCT)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

120986102

Gene

GRIK4

is a	snp
is	mentioned by
dbSNP	rs869312699
dbSNP (classic)	rs869312699
ClinGen	rs869312699
ebi	rs869312699
HLI	rs869312699
Exac	rs869312699
Gnomad	rs869312699
Varsome	rs869312699
LitVar	rs869312699
Map	rs869312699
PheGenI	rs869312699
Biobank	rs869312699
1000 genomes	rs869312699
hgdp	rs869312699
ensembl	rs869312699
geneview	rs869312699
scholar	rs869312699
google	rs869312699
pharmgkb	rs869312699
gwascentral	rs869312699
openSNP	rs869312699
23andMe	rs869312699
SNPshot	rs869312699
SNPdbe	rs869312699
MSV3d	rs869312699
GWAS Ctlg	rs869312699

Max Magnitude

0

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,