rs104893677

Orientation

plus

Stabilized

plus

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

Make rs104893677(C;T)

Make rs104893677(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

148741880

Gene

AGTR1

is a	snp
is	mentioned by
dbSNP	rs104893677
dbSNP (classic)	rs104893677
ClinGen	rs104893677
ebi	rs104893677
HLI	rs104893677
Exac	rs104893677
Gnomad	rs104893677
Varsome	rs104893677
LitVar	rs104893677
Map	rs104893677
PheGenI	rs104893677
Biobank	rs104893677
1000 genomes	rs104893677
hgdp	rs104893677
ensembl	rs104893677
geneview	rs104893677
scholar	rs104893677
google	rs104893677
pharmgkb	rs104893677
gwascentral	rs104893677
openSNP	rs104893677
23andMe	rs104893677
SNPshot	rs104893677
SNPdbe	rs104893677
MSV3d	rs104893677
GWAS Ctlg	rs104893677

Max Magnitude

0

OMIM	106165
Desc
Variant	0004
Related	also

ClinVar
Risk	rs104893677(T;T)
Alt	rs104893677(T;T)
Reference	Rs104893677(C;C)
Significance	Pathogenic
Disease	Renal dysplasia
Variation	info
Gene	AGTR1
CLNDBN	Renal dysplasia
Reversed	0
HGVS	NC_000003.11:g.148459667C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000019690.27,