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rs794726686

From SNPedia

Orientationminus
Make rs794726686(-;-)
Make rs794726686(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position38343603
GeneGPR179
is asnp
is mentioned by
dbSNPrs794726686
ebirs794726686
HLIrs794726686
Exacrs794726686
Varsomers794726686
Maprs794726686
PheGenIrs794726686
hapmaprs794726686
1000 genomesrs794726686
hgdprs794726686
ensemblrs794726686
gopubmedrs794726686
geneviewrs794726686
scholarrs794726686
googlers794726686
pharmgkbrs794726686
gwascentralrs794726686
openSNPrs794726686
23andMers794726686
23andMe allrs794726686
SNP Nexus

SNPshotrs794726686
SNPdbers794726686
MSV3drs794726686
GWAS Ctlgrs794726686
Max Magnitude
ClinVar
Risk rs794726686(;)
Alt rs794726686(;)
Reference rs794726686(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.36499486delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000024204.3,