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rs786205854

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205854(A;G)
Make rs786205854(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position50193600
GeneGNAT1
is asnp
is mentioned by
dbSNPrs786205854
ebirs786205854
HLIrs786205854
Exacrs786205854
Varsomers786205854
Maprs786205854
PheGenIrs786205854
hapmaprs786205854
1000 genomesrs786205854
hgdprs786205854
ensemblrs786205854
gopubmedrs786205854
geneviewrs786205854
scholarrs786205854
googlers786205854
pharmgkbrs786205854
gwascentralrs786205854
openSNPrs786205854
23andMers786205854
23andMe allrs786205854
SNP Nexus

SNPshotrs786205854
SNPdbers786205854
MSV3drs786205854
GWAS Ctlgrs786205854
Max Magnitude0
ClinVar
Risk rs786205854(G;G)
Alt rs786205854(G;G)
Reference rs786205854(A;A)
Significance Pathogenic
Disease Night blindness
Variation info
Gene GNAT1
CLNDBN Night blindness, congenital stationary, type 1g
Reversed 0
HGVS NC_000003.11:g.50231033A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000171141.3,