rs397509380

Orientation

plus

Stabilized

plus

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

Make rs397509380(-;-)

Make rs397509380(-;CT)

Reference

GRCh38 38.1/141

Chromosome

4

Position

109870287

Gene

LRIT3

is a	snp
is	mentioned by
dbSNP	rs397509380
dbSNP (classic)	rs397509380
ClinGen	rs397509380
ebi	rs397509380
HLI	rs397509380
Exac	rs397509380
Gnomad	rs397509380
Varsome	rs397509380
LitVar	rs397509380
Map	rs397509380
PheGenI	rs397509380
Biobank	rs397509380
1000 genomes	rs397509380
hgdp	rs397509380
ensembl	rs397509380
geneview	rs397509380
scholar	rs397509380
google	rs397509380
pharmgkb	rs397509380
gwascentral	rs397509380
openSNP	rs397509380
23andMe	rs397509380
SNPshot	rs397509380
SNPdbe	rs397509380
MSV3d	rs397509380
GWAS Ctlg	rs397509380

Max Magnitude

0

ClinVar
Risk	rs397509380(-;-)
Alt	rs397509380(-;-)
Reference	Rs397509380(CT;CT)
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.110791443_110791444delCT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000032636.3,