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rs876661408

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661408(C;T)
Make rs876661408(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position100484440
GeneCDC14A
is asnp
is mentioned by
dbSNPrs876661408
ebirs876661408
HLIrs876661408
Exacrs876661408
Varsomers876661408
Maprs876661408
PheGenIrs876661408
hapmaprs876661408
1000 genomesrs876661408
hgdprs876661408
ensemblrs876661408
gopubmedrs876661408
geneviewrs876661408
scholarrs876661408
googlers876661408
pharmgkbrs876661408
gwascentralrs876661408
openSNPrs876661408
23andMers876661408
23andMe allrs876661408
SNP Nexus

SNPshotrs876661408
SNPdbers876661408
MSV3drs876661408
GWAS Ctlgrs876661408
Max Magnitude0
ClinVar
Risk rs876661408(T;T)
Alt rs876661408(T;T)
Reference rs876661408(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene CDC14A
CLNDBN Deafness, autosomal recessive 105
Reversed 0
HGVS NC_000001.10:g.100949996C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000223951.1,