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rs770066665

From SNPedia

Orientationplus
Make rs770066665(-;-)
Make rs770066665(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position38337640
GeneGPR179
is asnp
is mentioned by
dbSNPrs770066665
ebirs770066665
HLIrs770066665
Exacrs770066665
Varsomers770066665
Maprs770066665
PheGenIrs770066665
hapmaprs770066665
1000 genomesrs770066665
hgdprs770066665
ensemblrs770066665
gopubmedrs770066665
geneviewrs770066665
scholarrs770066665
googlers770066665
pharmgkbrs770066665
gwascentralrs770066665
openSNPrs770066665
23andMers770066665
23andMe allrs770066665
SNP Nexus

SNPshotrs770066665
SNPdbers770066665
MSV3drs770066665
GWAS Ctlgrs770066665
Max Magnitude
ClinVar
Risk rs770066665(;)
Alt rs770066665(;)
Reference rs770066665(G;G)
Significance Pathogenic
Disease Congenital stationary night blindness
Variation info
Gene GPR179
CLNDBN Congenital stationary night blindness, type 1E
Reversed 0
HGVS NC_000017.10:g.36493523delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000024203.3,