rs267607140

Orientation

minus

Stabilized

minus

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

Make rs267607140(A;A)

Make rs267607140(A;T)

Reference

GRCh38 38.1/141

Chromosome

15

Position

31028454

Gene	LOC105370752, TRPM1

is a	snp
is	mentioned by
dbSNP	rs267607140
dbSNP (classic)	rs267607140
ClinGen	rs267607140
ebi	rs267607140
HLI	rs267607140
Exac	rs267607140
Gnomad	rs267607140
Varsome	rs267607140
LitVar	rs267607140
Map	rs267607140
PheGenI	rs267607140
Biobank	rs267607140
1000 genomes	rs267607140
hgdp	rs267607140
ensembl	rs267607140
geneview	rs267607140
scholar	rs267607140
google	rs267607140
pharmgkb	rs267607140
gwascentral	rs267607140
openSNP	rs267607140
23andMe	rs267607140
SNPshot	rs267607140
SNPdbe	rs267607140
MSV3d	rs267607140
GWAS Ctlg	rs267607140

Max Magnitude

0

ClinVar
Risk	rs267607140(A;A)
Alt	rs267607140(A;A)
Reference	Rs267607140(T;T)
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.31320657A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006603.4,