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rs776814755

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs776814755(C;T)
Make rs776814755(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position27851390
GeneOCA2
is asnp
is mentioned by
dbSNPrs776814755
dbSNP (old)rs776814755
ClinGenrs776814755
ebirs776814755
HLIrs776814755
Exacrs776814755
Gnomadrs776814755
Varsomers776814755
Maprs776814755
PheGenIrs776814755
Biobankrs776814755
1000 genomesrs776814755
hgdprs776814755
ensemblrs776814755
gopubmedrs776814755
geneviewrs776814755
scholarrs776814755
googlers776814755
pharmgkbrs776814755
gwascentralrs776814755
openSNPrs776814755
23andMers776814755
23andMe allrs776814755
SNPshotrs776814755
SNPdbers776814755
MSV3drs776814755
GWAS Ctlgrs776814755
Max Magnitude0
ClinVar
Risk rs776814755(T;T)
Alt rs776814755(T;T)
Reference Rs776814755(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OCA2
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.28096536C>T
CLNSRC
CLNACC RCV000493655.1,