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rs746559651

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs746559651(-;-)
Make rs746559651(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position111126286
GeneDRAM2
is asnp
is mentioned by
dbSNPrs746559651
ebirs746559651
HLIrs746559651
Exacrs746559651
Varsomers746559651
Maprs746559651
PheGenIrs746559651
hapmaprs746559651
1000 genomesrs746559651
hgdprs746559651
ensemblrs746559651
gopubmedrs746559651
geneviewrs746559651
scholarrs746559651
googlers746559651
pharmgkbrs746559651
gwascentralrs746559651
openSNPrs746559651
23andMers746559651
23andMe allrs746559651
SNP Nexus

SNPshotrs746559651
SNPdbers746559651
MSV3drs746559651
GWAS Ctlgrs746559651
Max Magnitude0
ClinVar
Risk rs746559651(;)
Alt rs746559651(;)
Reference rs746559651(C;C)
Significance Pathogenic
Disease Retinal dystrophy Cone-rod dystrophy 21
Variation info
Gene DRAM2
CLNDBN Retinal dystrophy Cone-rod dystrophy 21
Reversed 0
HGVS NC_000001.10:g.111668908delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000172832.1, RCV000186601.2,