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rs1057520055

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520055(A;A)
Make rs1057520055(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position137162734
GeneGRIN1
is asnp
is mentioned by
dbSNPrs1057520055
dbSNP (old)rs1057520055
ClinGenrs1057520055
ebirs1057520055
HLIrs1057520055
Exacrs1057520055
Gnomadrs1057520055
Varsomers1057520055
Maprs1057520055
PheGenIrs1057520055
Biobankrs1057520055
1000 genomesrs1057520055
hgdprs1057520055
ensemblrs1057520055
gopubmedrs1057520055
geneviewrs1057520055
scholarrs1057520055
googlers1057520055
pharmgkbrs1057520055
gwascentralrs1057520055
openSNPrs1057520055
23andMers1057520055
23andMe allrs1057520055
SNPshotrs1057520055
SNPdbers1057520055
MSV3drs1057520055
GWAS Ctlgrs1057520055
Max Magnitude0
ClinVar
Risk rs1057520055(A;A)
Alt rs1057520055(A;A)
Reference Rs1057520055(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.140057186C>A
CLNSRC
CLNACC RCV000442420.1,