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rs121908281

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908281(C;C)
Make rs121908281(C;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position3770767
GeneRAX2
is asnp
is mentioned by
dbSNPrs121908281
ebirs121908281
HLIrs121908281
Exacrs121908281
Varsomers121908281
Maprs121908281
PheGenIrs121908281
hapmaprs121908281
1000 genomesrs121908281
hgdprs121908281
ensemblrs121908281
gopubmedrs121908281
geneviewrs121908281
scholarrs121908281
googlers121908281
pharmgkbrs121908281
gwascentralrs121908281
openSNPrs121908281
23andMers121908281
23andMe allrs121908281
SNP Nexus

SNPshotrs121908281
SNPdbers121908281
MSV3drs121908281
GWAS Ctlgrs121908281
Max Magnitude0
OMIM610362
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908281(C;C)
Alt rs121908281(C;C)
Reference rs121908281(G;G)
Significance Pathogenic
Disease Cone-rod dystrophy 11
Variation info
Gene RAX2
CLNDBN Cone-rod dystrophy 11
Reversed 1
HGVS NC_000019.9:g.3770765C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000001300.4,