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rs786205611

From SNPedia

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Geno Mag Summary
(TGACA;TGACA) 0 common in clinvar
Make rs786205611(-;-)
Make rs786205611(-;TGACA)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position13124029
GeneOPTN
is asnp
is mentioned by
dbSNPrs786205611
ebirs786205611
HLIrs786205611
Exacrs786205611
Varsomers786205611
Maprs786205611
PheGenIrs786205611
hapmaprs786205611
1000 genomesrs786205611
hgdprs786205611
ensemblrs786205611
gopubmedrs786205611
geneviewrs786205611
scholarrs786205611
googlers786205611
pharmgkbrs786205611
gwascentralrs786205611
openSNPrs786205611
23andMers786205611
23andMe allrs786205611
SNP Nexus

SNPshotrs786205611
SNPdbers786205611
MSV3drs786205611
GWAS Ctlgrs786205611
Max Magnitude0
ClinVar
Risk rs786205611(;)
Alt rs786205611(;)
Reference rs786205611(TGACA;TGACA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene OPTN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.13166029_13166033delTGACA
CLNSRC
CLNACC RCV000171456.1,