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

rs786205664

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205664(A;T)
Make rs786205664(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position111120671
GeneDRAM2
is asnp
is mentioned by
dbSNPrs786205664
ebirs786205664
HLIrs786205664
Exacrs786205664
Varsomers786205664
Maprs786205664
PheGenIrs786205664
hapmaprs786205664
1000 genomesrs786205664
hgdprs786205664
ensemblrs786205664
gopubmedrs786205664
geneviewrs786205664
scholarrs786205664
googlers786205664
pharmgkbrs786205664
gwascentralrs786205664
openSNPrs786205664
23andMers786205664
23andMe allrs786205664
SNP Nexus

SNPshotrs786205664
SNPdbers786205664
MSV3drs786205664
GWAS Ctlgrs786205664
Max Magnitude0
ClinVar
Risk rs786205664(T;T)
Alt rs786205664(T;T)
Reference rs786205664(A;A)
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.111663293T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000172836.1, RCV000186605.2,