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rs1057518577

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs1057518577(GT;GT)
Make rs1057518577(GT;TA)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position13611722
GeneGRIN2B, LOC105369668
is asnp
is mentioned by
dbSNPrs1057518577
dbSNP (old)rs1057518577
ClinGenrs1057518577
ebirs1057518577
HLIrs1057518577
Exacrs1057518577
Gnomadrs1057518577
Varsomers1057518577
LitVarrs1057518577
Maprs1057518577
PheGenIrs1057518577
Biobankrs1057518577
1000 genomesrs1057518577
hgdprs1057518577
ensemblrs1057518577
gopubmedrs1057518577
geneviewrs1057518577
scholarrs1057518577
googlers1057518577
pharmgkbrs1057518577
gwascentralrs1057518577
openSNPrs1057518577
23andMers1057518577
23andMe allrs1057518577
SNPshotrs1057518577
SNPdbers1057518577
MSV3drs1057518577
GWAS Ctlgrs1057518577
Max Magnitude0
ClinVar
Risk rs1057518577(GT;GT)
Alt rs1057518577(GT;GT)
Reference Rs1057518577(TA;TA)
Significance Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.13764656_13764657delTAinsAC
CLNSRC
CLNACC RCV000414287.1,