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rs786205652

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205652(-;-)
Make rs786205652(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position65495232
GeneEYS
is asnp
is mentioned by
dbSNPrs786205652
ebirs786205652
HLIrs786205652
Exacrs786205652
Varsomers786205652
Maprs786205652
PheGenIrs786205652
hapmaprs786205652
1000 genomesrs786205652
hgdprs786205652
ensemblrs786205652
gopubmedrs786205652
geneviewrs786205652
scholarrs786205652
googlers786205652
pharmgkbrs786205652
gwascentralrs786205652
openSNPrs786205652
23andMers786205652
23andMe allrs786205652
SNP Nexus

SNPshotrs786205652
SNPdbers786205652
MSV3drs786205652
GWAS Ctlgrs786205652
Max Magnitude0
ClinVar
Risk rs786205652(;)
Alt rs786205652(;)
Reference rs786205652(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EYS
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.66205125delA
CLNSRC
CLNACC RCV000171525.1,