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rs587777209

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777209(C;T)
Make rs587777209(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position233328488
GeneSAG
is asnp
is mentioned by
dbSNPrs587777209
ebirs587777209
HLIrs587777209
Exacrs587777209
Varsomers587777209
Maprs587777209
PheGenIrs587777209
hapmaprs587777209
1000 genomesrs587777209
hgdprs587777209
ensemblrs587777209
gopubmedrs587777209
geneviewrs587777209
scholarrs587777209
googlers587777209
pharmgkbrs587777209
gwascentralrs587777209
openSNPrs587777209
23andMers587777209
23andMe allrs587777209
SNP Nexus

SNPshotrs587777209
SNPdbers587777209
MSV3drs587777209
GWAS Ctlgrs587777209
Max Magnitude0
ClinVar
Risk rs587777209(T;T)
Alt rs587777209(T;T)
Reference rs587777209(C;C)
Significance Pathogenic
Disease Oguchi's disease
Variation info
Gene SAG
CLNDBN Oguchi's disease
Reversed 0
HGVS NC_000002.11:g.234237134C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000088649.3,