rs121917813

Orientation

plus

Stabilized

plus

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

Make rs121917813(A;T)

Make rs121917813(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

116172437

Gene

AGTR2

is a	snp
is	mentioned by
dbSNP	rs121917813
dbSNP (classic)	rs121917813
ClinGen	rs121917813
ebi	rs121917813
HLI	rs121917813
Exac	rs121917813
Gnomad	rs121917813
Varsome	rs121917813
LitVar	rs121917813
Map	rs121917813
PheGenI	rs121917813
Biobank	rs121917813
1000 genomes	rs121917813
hgdp	rs121917813
ensembl	rs121917813
geneview	rs121917813
scholar	rs121917813
google	rs121917813
pharmgkb	rs121917813
gwascentral	rs121917813
openSNP	rs121917813
23andMe	rs121917813
SNPshot	rs121917813
SNPdbe	rs121917813
MSV3d	rs121917813
GWAS Ctlg	rs121917813

Max Magnitude

0

ClinVar
Risk	rs121917813(T;T)
Alt	rs121917813(T;T)
Reference	Rs121917813(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	AGTR2
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.115303690A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000088654.2,