rs145171629

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs145171629(A;A)

Make rs145171629(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

19

Position

53810801

Gene

NLRP12

is a	snp
is	mentioned by
dbSNP	rs145171629
dbSNP (classic)	rs145171629
ClinGen	rs145171629
ebi	rs145171629
HLI	rs145171629
Exac	rs145171629
Gnomad	rs145171629
Varsome	rs145171629
LitVar	rs145171629
Map	rs145171629
PheGenI	rs145171629
Biobank	rs145171629
1000 genomes	rs145171629
hgdp	rs145171629
ensembl	rs145171629
geneview	rs145171629
scholar	rs145171629
google	rs145171629
pharmgkb	rs145171629
gwascentral	rs145171629
openSNP	rs145171629
23andMe	rs145171629
SNPshot	rs145171629
SNPdbe	rs145171629
MSV3d	rs145171629
GWAS Ctlg	rs145171629

Max Magnitude

0

ClinVar
Risk	rs145171629(A;A) rs145171629(C;C)
Alt	rs145171629(A;A) rs145171629(C;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,