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rs786205662

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205662(C;C)
Make rs786205662(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position111131476
GeneDRAM2
is asnp
is mentioned by
dbSNPrs786205662
ebirs786205662
HLIrs786205662
Exacrs786205662
Varsomers786205662
Maprs786205662
PheGenIrs786205662
hapmaprs786205662
1000 genomesrs786205662
hgdprs786205662
ensemblrs786205662
gopubmedrs786205662
geneviewrs786205662
scholarrs786205662
googlers786205662
pharmgkbrs786205662
gwascentralrs786205662
openSNPrs786205662
23andMers786205662
23andMe allrs786205662
SNP Nexus

SNPshotrs786205662
SNPdbers786205662
MSV3drs786205662
GWAS Ctlgrs786205662
Max Magnitude0
ClinVar
Risk rs786205662(C;C)
Alt rs786205662(C;C)
Reference rs786205662(T;T)
Significance Pathogenic
Disease Retinal dystrophy
Variation info
Gene DRAM2
CLNDBN Retinal dystrophy
Reversed 1
HGVS NC_000001.10:g.111674098A>G
CLNSRC University of Leeds
CLNACC RCV000172834.1,