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

rs104893614

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893614(A;A)
Make rs104893614(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position98396018
GeneCNGA3
is asnp
is mentioned by
dbSNPrs104893614
ebirs104893614
HLIrs104893614
Exacrs104893614
Varsomers104893614
Maprs104893614
PheGenIrs104893614
hapmaprs104893614
1000 genomesrs104893614
hgdprs104893614
ensemblrs104893614
gopubmedrs104893614
geneviewrs104893614
scholarrs104893614
googlers104893614
pharmgkbrs104893614
gwascentralrs104893614
openSNPrs104893614
23andMers104893614
23andMe allrs104893614
SNP Nexus

SNPshotrs104893614
SNPdbers104893614
MSV3drs104893614
GWAS Ctlgrs104893614
Max Magnitude0
OMIM600053
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104893614(A;A)
Alt rs104893614(A;A)
Reference rs104893614(G;G)
Significance Pathogenic
Disease Achromatopsia 2
Variation info
Gene CNGA3
CLNDBN Achromatopsia 2
Reversed 0
HGVS NC_000002.11:g.99012481G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010083.3,