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rs397517331

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517331(-;-)
Make rs397517331(-;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position71439877
GeneCDH23
is asnp
is mentioned by
dbSNPrs397517331
ebirs397517331
HLIrs397517331
Exacrs397517331
Varsomers397517331
Maprs397517331
PheGenIrs397517331
hapmaprs397517331
1000 genomesrs397517331
hgdprs397517331
ensemblrs397517331
gopubmedrs397517331
geneviewrs397517331
scholarrs397517331
googlers397517331
pharmgkbrs397517331
gwascentralrs397517331
openSNPrs397517331
23andMers397517331
23andMe allrs397517331
SNP Nexus

SNPshotrs397517331
SNPdbers397517331
MSV3drs397517331
GWAS Ctlgrs397517331
Max Magnitude0
ClinVar
Risk rs397517331(;)
Alt rs397517331(;)
Reference rs397517331(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene CDH23
CLNDBN Usher syndrome, type 1D
Reversed 0
HGVS NC_000010.10:g.73199634delG
CLNSRC ClinVar
CLNACC RCV000039188.2,