rs267607141

Orientation

minus

Stabilized

minus

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

Make rs267607141(C;T)

Make rs267607141(T;T)

Reference

GRCh38 38.1/141

Chromosome

15

Position

31070213

Gene

TRPM1

is a	snp
is	mentioned by
dbSNP	rs267607141
dbSNP (classic)	rs267607141
ClinGen	rs267607141
ebi	rs267607141
HLI	rs267607141
Exac	rs267607141
Gnomad	rs267607141
Varsome	rs267607141
LitVar	rs267607141
Map	rs267607141
PheGenI	rs267607141
Biobank	rs267607141
1000 genomes	rs267607141
hgdp	rs267607141
ensembl	rs267607141
geneview	rs267607141
scholar	rs267607141
google	rs267607141
pharmgkb	rs267607141
gwascentral	rs267607141
openSNP	rs267607141
23andMe	rs267607141
SNPshot	rs267607141
SNPdbe	rs267607141
MSV3d	rs267607141
GWAS Ctlg	rs267607141

Max Magnitude

0

ClinVar
Risk	rs267607141(T;T)
Alt	rs267607141(T;T)
Reference	Rs267607141(C;C)
Significance	Pathogenic
Disease	Congenital stationary night blindness
Variation	info
Gene	TRPM1
CLNDBN	Congenital stationary night blindness, type 1C
Reversed	1
HGVS	NC_000015.9:g.31362416G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006604.3,