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rs74315337

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs74315337(C;T)
Make rs74315337(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position171652476
GeneMYOC
is asnp
is mentioned by
dbSNPrs74315337
ebirs74315337
HLIrs74315337
Exacrs74315337
Varsomers74315337
Maprs74315337
PheGenIrs74315337
hapmaprs74315337
1000 genomesrs74315337
hgdprs74315337
ensemblrs74315337
gopubmedrs74315337
geneviewrs74315337
scholarrs74315337
googlers74315337
pharmgkbrs74315337
gwascentralrs74315337
openSNPrs74315337
23andMers74315337
23andMe allrs74315337
SNP Nexus

SNPshotrs74315337
SNPdbers74315337
MSV3drs74315337
GWAS Ctlgrs74315337
GMAF0.002296
Max Magnitude0
OMIM601652
Desc
Variant0011
Relatedalso
ClinVar
Risk rs74315337(A,G,T;A,G,T)
Alt rs74315337(A,G,T;A,G,T)
Reference rs74315337(C;C)
Significance Pathogenic
Disease Glaucoma 1
Variation info
Gene MYOC
CLNDBN Glaucoma 1, open angle, a, autosomal recessive
Reversed 1
HGVS NC_000001.10:g.171621616G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008418.2,