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rs1064795493

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome2
Position51028155
GeneNRXN1
is asnp
is mentioned by
dbSNPrs1064795493
dbSNP (old)rs1064795493
ClinGenrs1064795493
ebirs1064795493
HLIrs1064795493
Exacrs1064795493
Gnomadrs1064795493
Varsomers1064795493
Maprs1064795493
PheGenIrs1064795493
Biobankrs1064795493
1000 genomesrs1064795493
hgdprs1064795493
ensemblrs1064795493
gopubmedrs1064795493
geneviewrs1064795493
scholarrs1064795493
googlers1064795493
pharmgkbrs1064795493
gwascentralrs1064795493
openSNPrs1064795493
23andMers1064795493
23andMe allrs1064795493
SNPshotrs1064795493
SNPdbers1064795493
MSV3drs1064795493
GWAS Ctlgrs1064795493
Max Magnitude0
ClinVar
Risk rs1064795493(A;A)
Alt rs1064795493(A;A)
Reference Rs1064795493(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NRXN1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.51255293C>T
CLNSRC
CLNACC RCV000484849.1,