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rs763721044

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs763721044(G;T)
Make rs763721044(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position71805836
GeneCDH23
is asnp
is mentioned by
dbSNPrs763721044
ebirs763721044
HLIrs763721044
Exacrs763721044
Varsomers763721044
Maprs763721044
PheGenIrs763721044
hapmaprs763721044
1000 genomesrs763721044
hgdprs763721044
ensemblrs763721044
gopubmedrs763721044
geneviewrs763721044
scholarrs763721044
googlers763721044
pharmgkbrs763721044
gwascentralrs763721044
openSNPrs763721044
23andMers763721044
23andMe allrs763721044
SNP Nexus

SNPshotrs763721044
SNPdbers763721044
MSV3drs763721044
GWAS Ctlgrs763721044
Max Magnitude0
ClinVar
Risk rs763721044(T;T)
Alt rs763721044(T;T)
Reference rs763721044(G;G)
Significance Pathogenic
Disease not specified Deafness
Variation info
Gene CDH23
CLNDBN not specified Deafness, autosomal recessive 12
Reversed 0
HGVS NC_000010.10:g.73565593G>T
CLNSRC
CLNACC RCV000216327.1, RCV000225060.1,