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rs121909128

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909128(C;G)
Make rs121909128(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position59269136
GeneRAX
is asnp
is mentioned by
dbSNPrs121909128
ebirs121909128
HLIrs121909128
Exacrs121909128
Varsomers121909128
Maprs121909128
PheGenIrs121909128
hapmaprs121909128
1000 genomesrs121909128
hgdprs121909128
ensemblrs121909128
gopubmedrs121909128
geneviewrs121909128
scholarrs121909128
googlers121909128
pharmgkbrs121909128
gwascentralrs121909128
openSNPrs121909128
23andMers121909128
23andMe allrs121909128
SNP Nexus

SNPshotrs121909128
SNPdbers121909128
MSV3drs121909128
GWAS Ctlgrs121909128
Max Magnitude0
OMIM601881
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121909128(G;G)
Alt rs121909128(G;G)
Reference rs121909128(C;C)
Significance Pathogenic
Disease Microphthalmia
Variation info
Gene RAX
CLNDBN Microphthalmia, isolated 3
Reversed 1
HGVS NC_000018.9:g.56936368G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000008077.4,