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rs786205665

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205665(A;A)
Make rs786205665(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position111131424
GeneDRAM2
is asnp
is mentioned by
dbSNPrs786205665
ebirs786205665
HLIrs786205665
Exacrs786205665
Varsomers786205665
Maprs786205665
PheGenIrs786205665
hapmaprs786205665
1000 genomesrs786205665
hgdprs786205665
ensemblrs786205665
gopubmedrs786205665
geneviewrs786205665
scholarrs786205665
googlers786205665
pharmgkbrs786205665
gwascentralrs786205665
openSNPrs786205665
23andMers786205665
23andMe allrs786205665
SNP Nexus

SNPshotrs786205665
SNPdbers786205665
MSV3drs786205665
GWAS Ctlgrs786205665
Max Magnitude0
ClinVar
Risk rs786205665(A;A)
Alt rs786205665(A;A)
Reference rs786205665(G;G)
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.111674046C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000172837.1, RCV000186603.2,