rs12424086

Orientation

plus

Stabilized

plus

Make rs12424086(C;C)

Make rs12424086(C;T)

Make rs12424086(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

65970729

is a	snp
is	mentioned by
dbSNP	rs12424086
dbSNP (classic)	rs12424086
ClinGen	rs12424086
ebi	rs12424086
HLI	rs12424086
Exac	rs12424086
Gnomad	rs12424086
Varsome	rs12424086
LitVar	rs12424086
Map	rs12424086
PheGenI	rs12424086
Biobank	rs12424086
1000 genomes	rs12424086
hgdp	rs12424086
ensembl	rs12424086
geneview	rs12424086
scholar	rs12424086
google	rs12424086
pharmgkb	rs12424086
gwascentral	rs12424086
openSNP	rs12424086
23andMe	rs12424086
SNPshot	rs12424086
SNPdbe	rs12424086
MSV3d	rs12424086
GWAS Ctlg	rs12424086

GMAF

0.1309

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 20195514]
Trait	Primary tooth development (number of teeth)
Title	Genome-Wide Association Study Reveals Multiple Loci Associated with Primary Tooth Development during Infancy
Risk Allele	C
P-val	0.000004
Odds Ratio	0.22 [NR] % variance explained

GWAS snp
PMID	[PMID 21931568]
Trait
Title	Genome-wide association study identifies four loci associated with eruption of permanent teeth.
Risk Allele	C
P-val	2E-12
Odds Ratio	0.1110 [0.08-0.14] unit decrease