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rs767489236

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CAGCGGTGATAAGGCCAA;CAGCGGTGATAAGGCCAA) 0 common in clinvar
Make rs767489236(-;-)
Make rs767489236(-;CAGCGGTGATAAGGCCAA)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position28022511
GeneOCA2
is asnp
is mentioned by
dbSNPrs767489236
dbSNP (old)rs767489236
ClinGenrs767489236
ebirs767489236
HLIrs767489236
Exacrs767489236
Gnomadrs767489236
Varsomers767489236
Maprs767489236
PheGenIrs767489236
Biobankrs767489236
1000 genomesrs767489236
hgdprs767489236
ensemblrs767489236
gopubmedrs767489236
geneviewrs767489236
scholarrs767489236
googlers767489236
pharmgkbrs767489236
gwascentralrs767489236
openSNPrs767489236
23andMers767489236
23andMe allrs767489236
SNPshotrs767489236
SNPdbers767489236
MSV3drs767489236
GWAS Ctlgrs767489236
Max Magnitude0
ClinVar
Risk rs767489236(-;-)
Alt rs767489236(-;-)
Reference Rs767489236(CAGCGGTGATAAGGCCAA;CAGCGGTGATAAGGCCAA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene OCA2
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.28267657_28267674del18
CLNSRC
CLNACC RCV000413670.1,