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rs1057517224

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517224(C;T)
Make rs1057517224(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position150972696
GeneCLRN1, CLRN1-AS1
is asnp
is mentioned by
dbSNPrs1057517224
dbSNP (classic)rs1057517224
ClinGenrs1057517224
ebirs1057517224
HLIrs1057517224
Exacrs1057517224
Gnomadrs1057517224
Varsomers1057517224
LitVarrs1057517224
Maprs1057517224
PheGenIrs1057517224
Biobankrs1057517224
1000 genomesrs1057517224
hgdprs1057517224
ensemblrs1057517224
geneviewrs1057517224
scholarrs1057517224
googlers1057517224
pharmgkbrs1057517224
gwascentralrs1057517224
openSNPrs1057517224
23andMers1057517224
SNPshotrs1057517224
SNPdbers1057517224
MSV3drs1057517224
GWAS Ctlgrs1057517224
Max Magnitude0
ClinVar
Risk rs1057517224(T;T)
Alt rs1057517224(T;T)
Reference Rs1057517224(C;C)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene CLRN1-AS1 CLRN1
CLNDBN Usher syndrome, type 3A
Reversed 1
HGVS NC_000003.11:g.150690483G>A
CLNSRC
CLNACC RCV000412180.1,