Have questions? Visit https://www.reddit.com/r/SNPedia

rs398124431

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124431(A;A)
Make rs398124431(A;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position3770832
GeneRAX2
is asnp
is mentioned by
dbSNPrs398124431
ebirs398124431
HLIrs398124431
Exacrs398124431
Varsomers398124431
Maprs398124431
PheGenIrs398124431
hapmaprs398124431
1000 genomesrs398124431
hgdprs398124431
ensemblrs398124431
gopubmedrs398124431
geneviewrs398124431
scholarrs398124431
googlers398124431
pharmgkbrs398124431
gwascentralrs398124431
openSNPrs398124431
23andMers398124431
23andMe allrs398124431
SNP Nexus

SNPshotrs398124431
SNPdbers398124431
MSV3drs398124431
GWAS Ctlgrs398124431
Max Magnitude0
ClinVar
Risk rs398124431(A;A)
Alt rs398124431(A;A)
Reference rs398124431(C;C)
Significance Pathogenic
Disease Age-related macular degeneration 6 Cone-rod dystrophy 11
Variation info
Gene RAX2
CLNDBN Age-related macular degeneration 6 Cone-rod dystrophy 11
Reversed 1
HGVS NC_000019.9:g.3770830G>T
CLNSRC ClinVar Emory University
CLNACC RCV000082311.4, RCV000177392.1,