rs1038426

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs1038426(A;A)

Make rs1038426(A;C)

Reference

GRCh38 38.1/141

Chromosome

4

Position

67737817

Gene

GNRHR

is a	snp
is	mentioned by
dbSNP	rs1038426
dbSNP (classic)	rs1038426
ClinGen	rs1038426
ebi	rs1038426
HLI	rs1038426
Exac	rs1038426
Gnomad	rs1038426
Varsome	rs1038426
LitVar	rs1038426
Map	rs1038426
PheGenI	rs1038426
Biobank	rs1038426
1000 genomes	rs1038426
hgdp	rs1038426
ensembl	rs1038426
geneview	rs1038426
scholar	rs1038426
google	rs1038426
pharmgkb	rs1038426
gwascentral	rs1038426
openSNP	rs1038426
23andMe	rs1038426
SNPshot	rs1038426
SNPdbe	rs1038426
MSV3d	rs1038426
GWAS Ctlg	rs1038426

GMAF

0.3572

Max Magnitude

0

?

(A;A) (A;C) (C;C)

28

[PMID 21274726] Common genetic variation in the 3'-untranslated region of gonadotropin-releasing hormone receptor regulates gene expression in cella and is associated with thyroid function, insulin secretion as well as insulin sensitivity in polycystic ovary syndrome patients.

ClinVar
Risk	rs1038426(A;A) rs1038426(T;T)
Alt	rs1038426(A;A) rs1038426(T;T)
Reference	Rs1038426(C;C)
Significance	Probable-non-pathogenic
Disease	Isolated GnRH Deficiency
Variation	info
Gene	GNRHR
CLNDBN	Isolated GnRH Deficiency
Reversed	0
HGVS	NC_000004.11:g.68603535C>A
CLNSRC
CLNACC	RCV000386570.1,