rs1804495

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar
(G;T)	0.1
(T;T)	0.3

Reference

GRCh38 38.1/141

Chromosome

X

Position

106034370

Gene

SERPINA7

is a	snp
is	mentioned by
dbSNP	rs1804495
dbSNP (classic)	rs1804495
ClinGen	rs1804495
ebi	rs1804495
HLI	rs1804495
Exac	rs1804495
Gnomad	rs1804495
Varsome	rs1804495
LitVar	rs1804495
Map	rs1804495
PheGenI	rs1804495
Biobank	rs1804495
1000 genomes	rs1804495
hgdp	rs1804495
ensembl	rs1804495
geneview	rs1804495
scholar	rs1804495
google	rs1804495
pharmgkb	rs1804495
gwascentral	rs1804495
openSNP	rs1804495
23andMe	rs1804495
SNPshot	rs1804495
SNPdbe	rs1804495
MSV3d	rs1804495
GWAS Ctlg	rs1804495

GMAF

0.1378

Max Magnitude

0.3

?	(G;G) (G;T) (T;T)	28

No known significance

OMIM	314200
Desc	THYROXINE-BINDING GLOBULIN, VARIANT P
Variant	0003
Related	also

ClinVar
Risk	Rs1804495(T;T)
Alt	Rs1804495(T;T)
Reference	Rs1804495(G;G)
Significance	Pathogenic
Disease	Thyroxine-binding globulin
Variation	info
Gene	SERPINA7
CLNDBN	Thyroxine-binding globulin, variant P
Reversed	1
HGVS	NC_000023.10:g.105278361C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000010442.3,