Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057520662

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520662(G;T)
Make rs1057520662(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position71803076
GeneCDH23
is asnp
is mentioned by
dbSNPrs1057520662
dbSNP (old)rs1057520662
ClinGenrs1057520662
ebirs1057520662
HLIrs1057520662
Exacrs1057520662
Gnomadrs1057520662
Varsomers1057520662
Maprs1057520662
PheGenIrs1057520662
Biobankrs1057520662
1000 genomesrs1057520662
hgdprs1057520662
ensemblrs1057520662
gopubmedrs1057520662
geneviewrs1057520662
scholarrs1057520662
googlers1057520662
pharmgkbrs1057520662
gwascentralrs1057520662
openSNPrs1057520662
23andMers1057520662
23andMe allrs1057520662
SNPshotrs1057520662
SNPdbers1057520662
MSV3drs1057520662
GWAS Ctlgrs1057520662
Max Magnitude0
ClinVar
Risk rs1057520662(T;T)
Alt rs1057520662(T;T)
Reference Rs1057520662(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CDH23
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.73562833G>T
CLNSRC
CLNACC RCV000421709.1,