rs35474657

Orientation

minus

Stabilized

minus

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

Make rs35474657(C;T)

Make rs35474657(T;T)

Reference

GRCh38 38.1/142

Chromosome

X

Position

116173251

Gene

AGTR2

is a	snp
is	mentioned by
dbSNP	rs35474657
dbSNP (classic)	rs35474657
ClinGen	rs35474657
ebi	rs35474657
HLI	rs35474657
Exac	rs35474657
Gnomad	rs35474657
Varsome	rs35474657
LitVar	rs35474657
Map	rs35474657
PheGenI	rs35474657
Biobank	rs35474657
1000 genomes	rs35474657
hgdp	rs35474657
ensembl	rs35474657
geneview	rs35474657
scholar	rs35474657
google	rs35474657
pharmgkb	rs35474657
gwascentral	rs35474657
openSNP	rs35474657
23andMe	rs35474657
SNPshot	rs35474657
SNPdbe	rs35474657
MSV3d	rs35474657
GWAS Ctlg	rs35474657

GMAF

0.002418

Max Magnitude

0

OMIM	300034
Desc
Variant	0003
Related	also

ClinVar
Risk	rs35474657(T;T)
Alt	rs35474657(T;T)
Reference	Rs35474657(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	AGTR2
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.115304504G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000088653.2,