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rs61732310

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61732310(C;T)
Make rs61732310(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position49061735
GeneNTF4
is asnp
is mentioned by
dbSNPrs61732310
ebirs61732310
HLIrs61732310
Exacrs61732310
Varsomers61732310
Maprs61732310
PheGenIrs61732310
hapmaprs61732310
1000 genomesrs61732310
hgdprs61732310
ensemblrs61732310
gopubmedrs61732310
geneviewrs61732310
scholarrs61732310
googlers61732310
pharmgkbrs61732310
gwascentralrs61732310
openSNPrs61732310
23andMers61732310
23andMe allrs61732310
SNP Nexus

SNPshotrs61732310
SNPdbers61732310
MSV3drs61732310
GWAS Ctlgrs61732310
GMAF0.001837
Max Magnitude0
OMIM162662
Desc
Variant0001
Relatedalso
ClinVar
Risk rs61732310(T;T)
Alt rs61732310(T;T)
Reference rs61732310(C;C)
Significance Pathogenic
Disease Glaucoma 1
Variation info
Gene NTF4
CLNDBN Glaucoma 1, open angle, O
Reversed 1
HGVS NC_000019.9:g.49564992G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015060.25,