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rs1057521798

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057521798(G;G)
Make rs1057521798(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position50497380
GeneNRXN1
is asnp
is mentioned by
dbSNPrs1057521798
dbSNP (old)rs1057521798
ClinGenrs1057521798
ebirs1057521798
HLIrs1057521798
Exacrs1057521798
Gnomadrs1057521798
Varsomers1057521798
Maprs1057521798
PheGenIrs1057521798
Biobankrs1057521798
1000 genomesrs1057521798
hgdprs1057521798
ensemblrs1057521798
gopubmedrs1057521798
geneviewrs1057521798
scholarrs1057521798
googlers1057521798
pharmgkbrs1057521798
gwascentralrs1057521798
openSNPrs1057521798
23andMers1057521798
23andMe allrs1057521798
SNPshotrs1057521798
SNPdbers1057521798
MSV3drs1057521798
GWAS Ctlgrs1057521798
Max Magnitude0
ClinVar
Risk rs1057521798(G;G)
Alt rs1057521798(G;G)
Reference Rs1057521798(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NRXN1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.50724518A>C
CLNSRC
CLNACC RCV000427988.1,