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rs104894663

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894663(C;T)
Make rs104894663(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position59272465
GeneRAX
is asnp
is mentioned by
dbSNPrs104894663
ebirs104894663
HLIrs104894663
Exacrs104894663
Varsomers104894663
Maprs104894663
PheGenIrs104894663
hapmaprs104894663
1000 genomesrs104894663
hgdprs104894663
ensemblrs104894663
gopubmedrs104894663
geneviewrs104894663
scholarrs104894663
googlers104894663
pharmgkbrs104894663
gwascentralrs104894663
openSNPrs104894663
23andMers104894663
23andMe allrs104894663
SNP Nexus

SNPshotrs104894663
SNPdbers104894663
MSV3drs104894663
GWAS Ctlgrs104894663
Max Magnitude0
OMIM601881
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894663(T;T)
Alt rs104894663(T;T)
Reference rs104894663(C;C)
Significance Pathogenic
Disease Microphthalmia
Variation info
Gene RAX
CLNDBN Microphthalmia, isolated 3
Reversed 1
HGVS NC_000018.9:g.56939697G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008074.4,