rs12734338

plus

Geno	Mag	Summary
(C;T)	1	Gender=Male (if data is from a DNA chip)
(T;T)	1	Gender=Female (if data is from a DNA chip)

Make rs12734338(C;C)

Reference

GRCh38 38.1/141

Chromosome

1

Position

202500595

Gene

PPP1R12B

is a	snp
is	mentioned by
dbSNP	rs12734338
dbSNP (classic)	rs12734338
ClinGen	rs12734338
ebi	rs12734338
HLI	rs12734338
Exac	rs12734338
Gnomad	rs12734338
Varsome	rs12734338
LitVar	rs12734338
Map	rs12734338
PheGenI	rs12734338
Biobank	rs12734338
1000 genomes	rs12734338
hgdp	rs12734338
ensembl	rs12734338
geneview	rs12734338
scholar	rs12734338
google	rs12734338
pharmgkb	rs12734338
gwascentral	rs12734338
openSNP	rs12734338
23andMe	rs12734338
SNPshot	rs12734338
SNPdbe	rs12734338
MSV3d	rs12734338
GWAS Ctlg	rs12734338

Max Magnitude

1

Due to homology between a region on the Y chromosome and chromosome 1, a genotyping test for rs12734338 will return a result of (C;T) when males are tested and a result of (T;T) when females are tested.[PMID 20018050 ],[PMID 22362730 ]

?

(C;C) (C;T) (T;T)

28

GWAS snp
PMID	[PMID 24778558 ]
Trait	Coronary heart disease
Title	RTN4 and FBXL17 Genes are Associated with Coronary Heart Disease in Genome-Wide Association Analysis of Lithuanian Families.
Risk Allele	G
P-val	3E-7
Odds Ratio	29.00 [3.95-212.9]

GWAS snp
PMID	[PMID 23936387 ]
Trait	Celiac disease
Title	A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease.
Risk Allele	C
P-val	3E-7
Odds Ratio	NR NR