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rs61744404

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61744404(C;G)
Make rs61744404(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position232525489
GeneCHRND, PRSS56
is asnp
is mentioned by
dbSNPrs61744404
ebirs61744404
HLIrs61744404
Exacrs61744404
Varsomers61744404
Maprs61744404
PheGenIrs61744404
hapmaprs61744404
1000 genomesrs61744404
hgdprs61744404
ensemblrs61744404
gopubmedrs61744404
geneviewrs61744404
scholarrs61744404
googlers61744404
pharmgkbrs61744404
gwascentralrs61744404
openSNPrs61744404
23andMers61744404
23andMe allrs61744404
SNP Nexus

SNPshotrs61744404
SNPdbers61744404
MSV3drs61744404
GWAS Ctlgrs61744404
GMAF0.02342
Max Magnitude0
ClinVar
Risk rs61744404(G;G)
Alt rs61744404(G;G)
Reference rs61744404(C;C)
Significance Pathogenic
Disease Microphthalmia
Variation info
Gene CHRND PRSS56
CLNDBN Microphthalmia, isolated 6
Reversed 0
HGVS NC_000002.11:g.233390199C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000024074.2,