rs397509378

Orientation

plus

Stabilized

plus

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

Make rs397509378(C;T)

Make rs397509378(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

109870067

Gene

LRIT3

is a	snp
is	mentioned by
dbSNP	rs397509378
dbSNP (classic)	rs397509378
ClinGen	rs397509378
ebi	rs397509378
HLI	rs397509378
Exac	rs397509378
Gnomad	rs397509378
Varsome	rs397509378
LitVar	rs397509378
Map	rs397509378
PheGenI	rs397509378
Biobank	rs397509378
1000 genomes	rs397509378
hgdp	rs397509378
ensembl	rs397509378
geneview	rs397509378
scholar	rs397509378
google	rs397509378
pharmgkb	rs397509378
gwascentral	rs397509378
openSNP	rs397509378
23andMe	rs397509378
SNPshot	rs397509378
SNPdbe	rs397509378
MSV3d	rs397509378
GWAS Ctlg	rs397509378

Max Magnitude

0

ClinVar
Risk	rs397509378(T;T)
Alt	rs397509378(T;T)
Reference	Rs397509378(C;C)
Significance	Pathogenic
Disease	Congenital stationary night blindness
Variation	info
Gene	LRIT3
CLNDBN	Congenital stationary night blindness, type 1F
Reversed	0
HGVS	NC_000004.11:g.110791223C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000032634.2,