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rs397517932

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GTCAT;GTCAT) 0 common in clinvar
Make rs397517932(-;-)
Make rs397517932(-;GTCAT)
ReferenceGRCh38 38.1/141
Chromosome3
Position150941710
GeneCLRN1
is asnp
is mentioned by
dbSNPrs397517932
ebirs397517932
HLIrs397517932
Exacrs397517932
Varsomers397517932
Maprs397517932
PheGenIrs397517932
hapmaprs397517932
1000 genomesrs397517932
hgdprs397517932
ensemblrs397517932
gopubmedrs397517932
geneviewrs397517932
scholarrs397517932
googlers397517932
pharmgkbrs397517932
gwascentralrs397517932
openSNPrs397517932
23andMers397517932
23andMe allrs397517932
SNP Nexus

SNPshotrs397517932
SNPdbers397517932
MSV3drs397517932
GWAS Ctlgrs397517932
Max Magnitude0
ClinVar
Risk rs397517932(;)
Alt rs397517932(;)
Reference rs397517932(GTCAT;GTCAT)
Significance Other
Disease Usher syndrome
Variation info
Gene CLRN1
CLNDBN Usher syndrome, type 3A
Reversed 1
HGVS NC_000003.11:g.150659497_150659501delATGAC
CLNSRC Counsyl
CLNACC RCV000041435.4,