Have questions? Visit https://www.reddit.com/r/SNPedia

rs1002820022

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1002820022(A;A)
Make rs1002820022(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position50054994
GeneNRXN1
is asnp
is mentioned by
dbSNPrs1002820022
dbSNP (classic)rs1002820022
ClinGenrs1002820022
ebirs1002820022
HLIrs1002820022
Exacrs1002820022
Gnomadrs1002820022
Varsomers1002820022
LitVarrs1002820022
Maprs1002820022
PheGenIrs1002820022
Biobankrs1002820022
1000 genomesrs1002820022
hgdprs1002820022
ensemblrs1002820022
geneviewrs1002820022
scholarrs1002820022
googlers1002820022
pharmgkbrs1002820022
gwascentralrs1002820022
openSNPrs1002820022
23andMers1002820022
23andMe allrs1002820022
SNPshotrs1002820022
SNPdbers1002820022
MSV3drs1002820022
GWAS Ctlgrs1002820022
Max Magnitude0
ClinVar
Risk rs1002820022(A;A) rs1002820022(T;T)
Alt rs1002820022(A;A) rs1002820022(T;T)
Reference Rs1002820022(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NRXN1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.50282132G>A
CLNSRC
CLNACC RCV000480371.1,