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rs1057516687

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057516687(-;T)
Make rs1057516687(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position150941579
GeneCLRN1
is asnp
is mentioned by
dbSNPrs1057516687
dbSNP (old)rs1057516687
ClinGenrs1057516687
ebirs1057516687
HLIrs1057516687
Exacrs1057516687
Gnomadrs1057516687
Varsomers1057516687
Maprs1057516687
PheGenIrs1057516687
Biobankrs1057516687
1000 genomesrs1057516687
hgdprs1057516687
ensemblrs1057516687
gopubmedrs1057516687
geneviewrs1057516687
scholarrs1057516687
googlers1057516687
pharmgkbrs1057516687
gwascentralrs1057516687
openSNPrs1057516687
23andMers1057516687
23andMe allrs1057516687
SNPshotrs1057516687
SNPdbers1057516687
MSV3drs1057516687
GWAS Ctlgrs1057516687
Max Magnitude0
ClinVar
Risk rs1057516687(T;T)
Alt rs1057516687(T;T)
Reference Rs1057516687(-;-)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene CLRN1
CLNDBN Usher syndrome, type 3A
Reversed 1
HGVS NC_000003.11:g.150659367dupA
CLNSRC
CLNACC RCV000412361.1,