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rs74315336

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs74315336(A;G)
Make rs74315336(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position171636173
GeneMYOC
is asnp
is mentioned by
dbSNPrs74315336
ebirs74315336
HLIrs74315336
Exacrs74315336
Varsomers74315336
Maprs74315336
PheGenIrs74315336
hapmaprs74315336
1000 genomesrs74315336
hgdprs74315336
ensemblrs74315336
gopubmedrs74315336
geneviewrs74315336
scholarrs74315336
googlers74315336
pharmgkbrs74315336
gwascentralrs74315336
openSNPrs74315336
23andMers74315336
23andMe allrs74315336
SNP Nexus

SNPshotrs74315336
SNPdbers74315336
MSV3drs74315336
GWAS Ctlgrs74315336
Max Magnitude0
OMIM601652
Desc
Variant0010
Relatedalso
ClinVar
Risk rs74315336(G;G)
Alt rs74315336(G;G)
Reference rs74315336(A;A)
Significance Pathogenic
Disease Primary open angle glaucoma juvenile onset 1
Variation info
Gene MYOC
CLNDBN Primary open angle glaucoma juvenile onset 1
Reversed 1
HGVS NC_000001.10:g.171605313T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000008417.4,