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rs796051861

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796051861(-;-)
Make rs796051861(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position71510129
GeneCDH23, LOC102723377
is asnp
is mentioned by
dbSNPrs796051861
ClinGenrs796051861
ebirs796051861
HLIrs796051861
Exacrs796051861
Varsomers796051861
Maprs796051861
PheGenIrs796051861
hapmaprs796051861
1000 genomesrs796051861
hgdprs796051861
ensemblrs796051861
gopubmedrs796051861
geneviewrs796051861
scholarrs796051861
googlers796051861
pharmgkbrs796051861
gwascentralrs796051861
openSNPrs796051861
23andMers796051861
23andMe allrs796051861
SNP Nexus

SNPshotrs796051861
SNPdbers796051861
MSV3drs796051861
GWAS Ctlgrs796051861
Max Magnitude0
ClinVar
Risk rs796051861(-;-)
Alt rs796051861(-;-)
Reference Rs796051861(C;C)
Significance Pathogenic
Disease Usher syndrome USHER SYNDROME Usher syndrome not provided
Variation info
Gene LOC102723377 CDH23
CLNDBN Usher syndrome, type 1D USHER SYNDROME, TYPE ID/F, DIGENIC Usher syndrome, type 1 not provided
Reversed 0
HGVS NC_000010.10:g.73269886delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000005207.4, RCV000005208.4, RCV000215123.1, RCV000254862.1,