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rs145171629

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs145171629(A;A)
Make rs145171629(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position53810801
GeneNLRP12
is asnp
is mentioned by
dbSNPrs145171629
ebirs145171629
HLIrs145171629
Exacrs145171629
Varsomers145171629
Maprs145171629
PheGenIrs145171629
hapmaprs145171629
1000 genomesrs145171629
hgdprs145171629
ensemblrs145171629
gopubmedrs145171629
geneviewrs145171629
scholarrs145171629
googlers145171629
pharmgkbrs145171629
gwascentralrs145171629
openSNPrs145171629
23andMers145171629
23andMe allrs145171629
SNP Nexus

SNPshotrs145171629
SNPdbers145171629
MSV3drs145171629
GWAS Ctlgrs145171629
Max Magnitude0
ClinVar
Risk rs145171629(A,C;A,C)
Alt rs145171629(A,C;A,C)
Reference rs145171629(G;G)
Significance Probable-Pathogenic
Disease Childhood-Onset Schizophrenia
Variation info
Gene NLRP12
CLNDBN Childhood-Onset Schizophrenia
Reversed 0
HGVS NC_000019.9:g.54314055G>C
CLNSRC
CLNACC RCV000202334.1,