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rs786205661

From SNPedia

Orientationminus
Geno Mag Summary
(GCT;GCT) 0 common in clinvar
Make rs786205661(-;-)
Make rs786205661(-;GCT)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position111131489
GeneDRAM2
is asnp
is mentioned by
dbSNPrs786205661
ebirs786205661
HLIrs786205661
Exacrs786205661
Varsomers786205661
Maprs786205661
PheGenIrs786205661
hapmaprs786205661
1000 genomesrs786205661
hgdprs786205661
ensemblrs786205661
gopubmedrs786205661
geneviewrs786205661
scholarrs786205661
googlers786205661
pharmgkbrs786205661
gwascentralrs786205661
openSNPrs786205661
23andMers786205661
23andMe allrs786205661
SNP Nexus

SNPshotrs786205661
SNPdbers786205661
MSV3drs786205661
GWAS Ctlgrs786205661
Max Magnitude0
ClinVar
Risk rs786205661(;)
Alt rs786205661(;)
Reference rs786205661(GCT;GCT)
Significance Pathogenic
Disease Retinal dystrophy Cone-rod dystrophy 21
Variation info
Gene DRAM2
CLNDBN Retinal dystrophy Cone-rod dystrophy 21
Reversed 1
HGVS NC_000001.10:g.111674111_111674113delAGC
CLNSRC OMIM Allelic Variant
CLNACC RCV000172833.1, RCV000186604.2,