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rs1057520406

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520406(A;G)
Make rs1057520406(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position50091496
GeneNRXN1
is asnp
is mentioned by
dbSNPrs1057520406
dbSNP (old)rs1057520406
ClinGenrs1057520406
ebirs1057520406
HLIrs1057520406
Exacrs1057520406
Gnomadrs1057520406
Varsomers1057520406
Maprs1057520406
PheGenIrs1057520406
Biobankrs1057520406
1000 genomesrs1057520406
hgdprs1057520406
ensemblrs1057520406
gopubmedrs1057520406
geneviewrs1057520406
scholarrs1057520406
googlers1057520406
pharmgkbrs1057520406
gwascentralrs1057520406
openSNPrs1057520406
23andMers1057520406
23andMe allrs1057520406
SNPshotrs1057520406
SNPdbers1057520406
MSV3drs1057520406
GWAS Ctlgrs1057520406
Max Magnitude0
ClinVar
Risk rs1057520406(G;G)
Alt rs1057520406(G;G)
Reference Rs1057520406(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NRXN1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.50318634T>C
CLNSRC
CLNACC RCV000441331.1,