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rs879253773

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879253773(A;A)
Make rs879253773(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position6846892
GeneCDCA3, GNB3
is asnp
is mentioned by
dbSNPrs879253773
ebirs879253773
HLIrs879253773
Exacrs879253773
Varsomers879253773
Maprs879253773
PheGenIrs879253773
hapmaprs879253773
1000 genomesrs879253773
hgdprs879253773
ensemblrs879253773
gopubmedrs879253773
geneviewrs879253773
scholarrs879253773
googlers879253773
pharmgkbrs879253773
gwascentralrs879253773
openSNPrs879253773
23andMers879253773
23andMe allrs879253773
SNP Nexus

SNPshotrs879253773
SNPdbers879253773
MSV3drs879253773
GWAS Ctlgrs879253773
Max Magnitude0
ClinVar
Risk rs879253773(A;A)
Alt rs879253773(A;A)
Reference rs879253773(G;G)
Significance Pathogenic
Disease Night blindness
Variation info
Gene GNB3 CDCA3
CLNDBN Night blindness, congenital stationary, type 1h
Reversed 0
HGVS NC_000012.11:g.6956056G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000234969.2,