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rs121908280

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908280(A;A)
Make rs121908280(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position3770916
GeneRAX2
is asnp
is mentioned by
dbSNPrs121908280
ebirs121908280
HLIrs121908280
Exacrs121908280
Varsomers121908280
Maprs121908280
PheGenIrs121908280
hapmaprs121908280
1000 genomesrs121908280
hgdprs121908280
ensemblrs121908280
gopubmedrs121908280
geneviewrs121908280
scholarrs121908280
googlers121908280
pharmgkbrs121908280
gwascentralrs121908280
openSNPrs121908280
23andMers121908280
23andMe allrs121908280
SNP Nexus

SNPshotrs121908280
SNPdbers121908280
MSV3drs121908280
GWAS Ctlgrs121908280
Max Magnitude0
OMIM610362
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908280(A;A)
Alt rs121908280(A;A)
Reference rs121908280(G;G)
Significance Pathogenic
Disease Age-related macular degeneration 6
Variation info
Gene RAX2
CLNDBN Age-related macular degeneration 6
Reversed 1
HGVS NC_000019.9:g.3770914C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001299.4,