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rs878854408

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878854408(C;C)
Make rs878854408(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position171636329
GeneMYOC
is asnp
is mentioned by
dbSNPrs878854408
ebirs878854408
HLIrs878854408
Exacrs878854408
Varsomers878854408
Maprs878854408
PheGenIrs878854408
hapmaprs878854408
1000 genomesrs878854408
hgdprs878854408
ensemblrs878854408
gopubmedrs878854408
geneviewrs878854408
scholarrs878854408
googlers878854408
pharmgkbrs878854408
gwascentralrs878854408
openSNPrs878854408
23andMers878854408
23andMe allrs878854408
SNP Nexus

SNPshotrs878854408
SNPdbers878854408
MSV3drs878854408
GWAS Ctlgrs878854408
Max Magnitude0
ClinVar
Risk rs878854408(C;C)
Alt rs878854408(C;C)
Reference rs878854408(T;T)
Significance Pathogenic
Disease Primary open angle glaucoma
Variation info
Gene MYOC
CLNDBN Primary open angle glaucoma
Reversed 1
HGVS NC_000001.10:g.171605469A>G
CLNSRC
CLNACC RCV000233750.1,