rs9321637

plus

Geno	Mag	Summary
(T;T)	0	common in complete genomics

Make rs9321637(C;C)

Make rs9321637(C;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

137945548

Gene	LOC105378020

is a	snp
is	mentioned by
dbSNP	rs9321637
dbSNP (classic)	rs9321637
ClinGen	rs9321637
ebi	rs9321637
HLI	rs9321637
Exac	rs9321637
Gnomad	rs9321637
Varsome	rs9321637
LitVar	rs9321637
Map	rs9321637
PheGenI	rs9321637
Biobank	rs9321637
1000 genomes	rs9321637
hgdp	rs9321637
ensembl	rs9321637
geneview	rs9321637
scholar	rs9321637
google	rs9321637
pharmgkb	rs9321637
gwascentral	rs9321637
openSNP	rs9321637
23andMe	rs9321637
SNPshot	rs9321637
SNPdbe	rs9321637
MSV3d	rs9321637
GWAS Ctlg	rs9321637

GMAF

0.1391

Max Magnitude

0

?

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

28

[PMID 22355377 ] Caucasian and asian specific rheumatoid arthritis risk Loci reveal limited replication and apparent allelic heterogeneity in north indians

GWAS snp
PMID	[PMID 23247143 ]
Trait	Cardiac Troponin-T levels
Title	Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European americans and blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.
Risk Allele	C
P-val	8E-6
Odds Ratio	2.17 [1.56-3.13]