rs121917810

Orientation

plus

Stabilized

plus

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

Make rs121917810(G;T)

Make rs121917810(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

116172342

Gene

AGTR2

is a	snp
is	mentioned by
dbSNP	rs121917810
dbSNP (classic)	rs121917810
ClinGen	rs121917810
ebi	rs121917810
HLI	rs121917810
Exac	rs121917810
Gnomad	rs121917810
Varsome	rs121917810
LitVar	rs121917810
Map	rs121917810
PheGenI	rs121917810
Biobank	rs121917810
1000 genomes	rs121917810
hgdp	rs121917810
ensembl	rs121917810
geneview	rs121917810
scholar	rs121917810
google	rs121917810
pharmgkb	rs121917810
gwascentral	rs121917810
openSNP	rs121917810
23andMe	rs121917810
SNPshot	rs121917810
SNPdbe	rs121917810
MSV3d	rs121917810
GWAS Ctlg	rs121917810

Max Magnitude

0

ClinVar
Risk	rs121917810(T;T)
Alt	rs121917810(T;T)
Reference	Rs121917810(G;G)
Significance	Non-pathogenic
Disease	not provided not specified
Variation	info
Gene	AGTR2
CLNDBN	not provided not specified
Reversed	0
HGVS	NC_000023.10:g.115303595G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000088651.2, RCV000116283.1,