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rs879253774

From SNPedia

Orientationplus
Geno Mag Summary
(AAG;AAG) 0 common in clinvar
Make rs879253774(-;-)
Make rs879253774(-;AGA)
Make rs879253774(AGA;AGA)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position6843043
GeneGNB3
is asnp
is mentioned by
dbSNPrs879253774
ebirs879253774
HLIrs879253774
Exacrs879253774
Varsomers879253774
Maprs879253774
PheGenIrs879253774
hapmaprs879253774
1000 genomesrs879253774
hgdprs879253774
ensemblrs879253774
gopubmedrs879253774
geneviewrs879253774
scholarrs879253774
googlers879253774
pharmgkbrs879253774
gwascentralrs879253774
openSNPrs879253774
23andMers879253774
23andMe allrs879253774
SNP Nexus

SNPshotrs879253774
SNPdbers879253774
MSV3drs879253774
GWAS Ctlgrs879253774
Max Magnitude0
ClinVar
Risk rs879253774(;)
Alt rs879253774(;)
Reference rs879253774(AAG;AAG)
Significance Pathogenic
Disease Night blindness
Variation info
Gene GNB3
CLNDBN Night blindness, congenital stationary, type 1h
Reversed 0
HGVS NC_000012.11:g.6952207_6952209delAGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000234964.2,