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rs794726685

From SNPedia

Orientationminus
Make rs794726685(-;-)
Make rs794726685(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position38343512
GeneGPR179
is asnp
is mentioned by
dbSNPrs794726685
ebirs794726685
HLIrs794726685
Exacrs794726685
Varsomers794726685
Maprs794726685
PheGenIrs794726685
hapmaprs794726685
1000 genomesrs794726685
hgdprs794726685
ensemblrs794726685
gopubmedrs794726685
geneviewrs794726685
scholarrs794726685
googlers794726685
pharmgkbrs794726685
gwascentralrs794726685
openSNPrs794726685
23andMers794726685
23andMe allrs794726685
SNP Nexus

SNPshotrs794726685
SNPdbers794726685
MSV3drs794726685
GWAS Ctlgrs794726685
Max Magnitude
ClinVar
Risk rs794726685(;)
Alt rs794726685(;)
Reference rs794726685(C;C)
Significance Pathogenic
Disease Congenital stationary night blindness
Variation info
Gene GPR179
CLNDBN Congenital stationary night blindness, type 1E
Reversed 1
HGVS NC_000017.10:g.36499395delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000024200.3,