rs10499559

Orientation

minus

Stabilized

minus

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

Make rs10499559(C;T)

Make rs10499559(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

22069841

is a	snp
is	mentioned by
dbSNP	rs10499559
dbSNP (classic)	rs10499559
ClinGen	rs10499559
ebi	rs10499559
HLI	rs10499559
Exac	rs10499559
Gnomad	rs10499559
Varsome	rs10499559
LitVar	rs10499559
Map	rs10499559
PheGenI	rs10499559
Biobank	rs10499559
1000 genomes	rs10499559
hgdp	rs10499559
ensembl	rs10499559
geneview	rs10499559
scholar	rs10499559
google	rs10499559
pharmgkb	rs10499559
gwascentral	rs10499559
openSNP	rs10499559
23andMe	rs10499559
SNPshot	rs10499559
SNPdbe	rs10499559
MSV3d	rs10499559
GWAS Ctlg	rs10499559

GMAF

0.1703

Max Magnitude

0

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

GWAS
SNP	rs10499559
PubMedID	[PMID 17903292]
Condition	Thyroid stimulating hormone
Gene	RAPGEF5
Risk Allele
pValue	8.00E-006
OR	NA
95% CI