rs7775698

Orientation

plus

Stabilized

plus

Make rs7775698(C;C)

Make rs7775698(C;T)

Make rs7775698(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

135097497

is a	snp
is	mentioned by
dbSNP	rs7775698
dbSNP (classic)	rs7775698
ClinGen	rs7775698
ebi	rs7775698
HLI	rs7775698
Exac	rs7775698
Gnomad	rs7775698
Varsome	rs7775698
LitVar	rs7775698
Map	rs7775698
PheGenI	rs7775698
Biobank	rs7775698
1000 genomes	rs7775698
hgdp	rs7775698
ensembl	rs7775698
geneview	rs7775698
scholar	rs7775698
google	rs7775698
pharmgkb	rs7775698
gwascentral	rs7775698
openSNP	rs7775698
23andMe	rs7775698
SNPshot	rs7775698
SNPdbe	rs7775698
MSV3d	rs7775698
GWAS Ctlg	rs7775698

Max Magnitude

0

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

GWAS snp
PMID	[PMID 20139978]
Trait	Hematological and biochemical traits
Title	Genome-wide association study of hematological and biochemical traits in a Japanese population
Risk Allele	T
P-val	3E-66
Odds Ratio	2.01 [NR] % variance

GWAS snp
PMID	[PMID 19853236]
Trait	Hematology traits
Title	Sequence variants in three loci influence monocyte counts and erythrocyte volume
Risk Allele	C
P-val	5E-13
Odds Ratio	0.19 [0.13-0.25] s.d. decrease

GWAS snp
PMID	[PMID 20927387]
Trait
Title	A genome-wide association study of red blood cell traits using the electronic medical record
Risk Allele	T
P-val	1E-14
Odds Ratio	0.09 [0.07-0.11] unit decrease

GWAS snp
PMID	[PMID 23263863]
Trait	Mean corpuscular volume
Title	GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.
Risk Allele	T
P-val	2E-9
Odds Ratio	.54 [0.37-0.72] unit increase