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rs35445598

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs35445598(A;A)
Make rs35445598(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position72233802
GeneRIMS1
is asnp
is mentioned by
dbSNPrs35445598
ebirs35445598
HLIrs35445598
Exacrs35445598
Varsomers35445598
Maprs35445598
PheGenIrs35445598
hapmaprs35445598
1000 genomesrs35445598
hgdprs35445598
ensemblrs35445598
gopubmedrs35445598
geneviewrs35445598
scholarrs35445598
googlers35445598
pharmgkbrs35445598
gwascentralrs35445598
openSNPrs35445598
23andMers35445598
23andMe allrs35445598
SNP Nexus

SNPshotrs35445598
SNPdbers35445598
MSV3drs35445598
GWAS Ctlgrs35445598
Max Magnitude0
Venter snp
Source plos
Gene RIMS1
allele A
frequency
sift TOLERATED
HuRef 1103652900145
Disease Association Defects in RIMS1 are a cause of autosomal dominant cone- rod dystrophy (CORD7) (MIM:603649). CORD7 is characterized by early loss of visual acuity and color vision, followed by night blindness and peripheral visual field loss. The onset of reduced color vision and visual acuity varies between the ages of 20 and 40 years.