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rs1057518520

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518520(-;GCTC)
Make rs1057518520(GCTC;GCTC)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position13564228
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs1057518520
dbSNP (classic)rs1057518520
ClinGenrs1057518520
ebirs1057518520
HLIrs1057518520
Exacrs1057518520
Gnomadrs1057518520
Varsomers1057518520
LitVarrs1057518520
Maprs1057518520
PheGenIrs1057518520
Biobankrs1057518520
1000 genomesrs1057518520
hgdprs1057518520
ensemblrs1057518520
geneviewrs1057518520
scholarrs1057518520
googlers1057518520
pharmgkbrs1057518520
gwascentralrs1057518520
openSNPrs1057518520
23andMers1057518520
23andMe allrs1057518520
SNPshotrs1057518520
SNPdbers1057518520
MSV3drs1057518520
GWAS Ctlgrs1057518520
Max Magnitude0
ClinVar
Risk rs1057518520(GCTC;GCTC)
Alt rs1057518520(GCTC;GCTC)
Reference Rs1057518520(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.13717163_13717166dupGAGC
CLNSRC
CLNACC RCV000413196.1,