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

rs786205612

From SNPedia

Orientationplus
Geno Mag Summary
(CCG;CCG) 0 common in clinvar
Make rs786205612(-;-)
Make rs786205612(-;CCG)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position71810549
GeneCDH23
is asnp
is mentioned by
dbSNPrs786205612
ebirs786205612
HLIrs786205612
Exacrs786205612
Varsomers786205612
Maprs786205612
PheGenIrs786205612
hapmaprs786205612
1000 genomesrs786205612
hgdprs786205612
ensemblrs786205612
gopubmedrs786205612
geneviewrs786205612
scholarrs786205612
googlers786205612
pharmgkbrs786205612
gwascentralrs786205612
openSNPrs786205612
23andMers786205612
23andMe allrs786205612
SNP Nexus

SNPshotrs786205612
SNPdbers786205612
MSV3drs786205612
GWAS Ctlgrs786205612
Max Magnitude0
ClinVar
Risk rs786205612(;)
Alt rs786205612(;)
Reference rs786205612(CCG;CCG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CDH23
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.73570306_73570308delCCG
CLNSRC
CLNACC RCV000171457.1,