rs1057521112

Orientation

plus

Stabilized

plus

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

Make rs1057521112(C;C)

Make rs1057521112(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

129528996

Gene

RHO

is a	snp
is	mentioned by
dbSNP	rs1057521112
dbSNP (classic)	rs1057521112
ClinGen	rs1057521112
ebi	rs1057521112
HLI	rs1057521112
Exac	rs1057521112
Gnomad	rs1057521112
Varsome	rs1057521112
LitVar	rs1057521112
Map	rs1057521112
PheGenI	rs1057521112
Biobank	rs1057521112
1000 genomes	rs1057521112
hgdp	rs1057521112
ensembl	rs1057521112
geneview	rs1057521112
scholar	rs1057521112
google	rs1057521112
pharmgkb	rs1057521112
gwascentral	rs1057521112
openSNP	rs1057521112
23andMe	rs1057521112
SNPshot	rs1057521112
SNPdbe	rs1057521112
MSV3d	rs1057521112
GWAS Ctlg	rs1057521112

Max Magnitude

0

ClinVar
Risk	rs1057521112(C;C)
Alt	rs1057521112(C;C)
Reference	Rs1057521112(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	RHO
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.129247839T>C
CLNSRC
CLNACC	RCV000442591.1,