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rs727504455

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504455(C;T)
Make rs727504455(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position71646537
GeneCDH23
is asnp
is mentioned by
dbSNPrs727504455
ebirs727504455
HLIrs727504455
Exacrs727504455
Varsomers727504455
Maprs727504455
PheGenIrs727504455
hapmaprs727504455
1000 genomesrs727504455
hgdprs727504455
ensemblrs727504455
gopubmedrs727504455
geneviewrs727504455
scholarrs727504455
googlers727504455
pharmgkbrs727504455
gwascentralrs727504455
openSNPrs727504455
23andMers727504455
23andMe allrs727504455
SNP Nexus

SNPshotrs727504455
SNPdbers727504455
MSV3drs727504455
GWAS Ctlgrs727504455
Max Magnitude0
ClinVar
Risk rs727504455(T;T)
Alt rs727504455(T;T)
Reference rs727504455(C;C)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene CDH23
CLNDBN Usher syndrome, type 1D
Reversed 0
HGVS NC_000010.10:g.73406294C>T
CLNSRC
CLNACC RCV000155432.1,