Have questions? Visit https://www.reddit.com/r/SNPedia

rs150115958

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs150115958(C;T)
Make rs150115958(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position67457677
GeneCABP4
is asnp
is mentioned by
dbSNPrs150115958
ebirs150115958
HLIrs150115958
Exacrs150115958
Varsomers150115958
Maprs150115958
PheGenIrs150115958
hapmaprs150115958
1000 genomesrs150115958
hgdprs150115958
ensemblrs150115958
gopubmedrs150115958
geneviewrs150115958
scholarrs150115958
googlers150115958
pharmgkbrs150115958
gwascentralrs150115958
openSNPrs150115958
23andMers150115958
23andMe allrs150115958
SNP Nexus

SNPshotrs150115958
SNPdbers150115958
MSV3drs150115958
GWAS Ctlgrs150115958
Max Magnitude0
ClinVar
Risk rs150115958(A,T;A,T)
Alt rs150115958(A,T;A,T)
Reference rs150115958(C;C)
Significance Pathogenic
Disease Congenital stationary night blindness
Variation info
Gene CABP4
CLNDBN Congenital stationary night blindness, type 2B
Reversed 0
HGVS NC_000011.9:g.67225148C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000171132.3,