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rs796052787

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052787(-;-)
Make rs796052787(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position50496087
GeneNRXN1
is asnp
is mentioned by
dbSNPrs796052787
ebirs796052787
HLIrs796052787
Exacrs796052787
Varsomers796052787
Maprs796052787
PheGenIrs796052787
hapmaprs796052787
1000 genomesrs796052787
hgdprs796052787
ensemblrs796052787
gopubmedrs796052787
geneviewrs796052787
scholarrs796052787
googlers796052787
pharmgkbrs796052787
gwascentralrs796052787
openSNPrs796052787
23andMers796052787
23andMe allrs796052787
SNP Nexus

SNPshotrs796052787
SNPdbers796052787
MSV3drs796052787
GWAS Ctlgrs796052787
Max Magnitude0
ClinVar
Risk rs796052787(;)
Alt rs796052787(;)
Reference rs796052787(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene NRXN1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.50723225delT
CLNSRC
CLNACC RCV000188305.1,