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rs786204428

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CAGG;CAGG) 0 common in clinvar
Make rs786204428(CAGG;TGTCCAAT)
Make rs786204428(TGTCCAAT;TGTCCAAT)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position150972557
GeneCLRN1, CLRN1-AS1
is asnp
is mentioned by
dbSNPrs786204428
dbSNP (classic)rs786204428
ClinGenrs786204428
ebirs786204428
HLIrs786204428
Exacrs786204428
Gnomadrs786204428
Varsomers786204428
LitVarrs786204428
Maprs786204428
PheGenIrs786204428
Biobankrs786204428
1000 genomesrs786204428
hgdprs786204428
ensemblrs786204428
geneviewrs786204428
scholarrs786204428
googlers786204428
pharmgkbrs786204428
gwascentralrs786204428
openSNPrs786204428
23andMers786204428
SNPshotrs786204428
SNPdbers786204428
MSV3drs786204428
GWAS Ctlgrs786204428
Max Magnitude0
ClinVar
Risk rs786204428(TGTCCAAT;TGTCCAAT)
Alt rs786204428(TGTCCAAT;TGTCCAAT)
Reference Rs786204428(CAGG;CAGG)
Significance Other
Disease Usher syndrome not provided
Variation info
Gene CLRN1-AS1 CLRN1
CLNDBN Usher syndrome, type 3A not provided
Reversed 1
HGVS NC_000003.11:g.150690344_150690347delCCTGinsATTGGACA
CLNSRC
CLNACC RCV000169027.2, RCV000478734.1,