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rs786205663

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(GTTCGTTAT;GTTCGTTAT) 0 common in clinvar
Make rs786205663(-;-)
Make rs786205663(-;GTTCGTTAT)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position111124856
GeneDRAM2
is asnp
is mentioned by
dbSNPrs786205663
dbSNP (old)rs786205663
ClinGenrs786205663
ebirs786205663
HLIrs786205663
Exacrs786205663
Gnomadrs786205663
Varsomers786205663
Maprs786205663
PheGenIrs786205663
Biobankrs786205663
1000 genomesrs786205663
hgdprs786205663
ensemblrs786205663
gopubmedrs786205663
geneviewrs786205663
scholarrs786205663
googlers786205663
pharmgkbrs786205663
gwascentralrs786205663
openSNPrs786205663
23andMers786205663
23andMe allrs786205663
SNP Nexus

SNPshotrs786205663
SNPdbers786205663
MSV3drs786205663
GWAS Ctlgrs786205663
Max Magnitude0
ClinVar
Risk rs786205663(-;-)
Alt rs786205663(-;-)
Reference Rs786205663(GTTCGTTAT;GTTCGTTAT)
Significance Pathogenic
Disease Retinal dystrophy
Variation info
Gene DRAM2
CLNDBN Retinal dystrophy
Reversed 1
HGVS NC_000001.10:g.111667478_111667486delATAACGAAC
CLNSRC University of Leeds
CLNACC RCV000172835.1,