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rs777112652

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs777112652(C;T)
Make rs777112652(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position100484329
GeneCDC14A
is asnp
is mentioned by
dbSNPrs777112652
ebirs777112652
HLIrs777112652
Exacrs777112652
Varsomers777112652
Maprs777112652
PheGenIrs777112652
hapmaprs777112652
1000 genomesrs777112652
hgdprs777112652
ensemblrs777112652
gopubmedrs777112652
geneviewrs777112652
scholarrs777112652
googlers777112652
pharmgkbrs777112652
gwascentralrs777112652
openSNPrs777112652
23andMers777112652
23andMe allrs777112652
SNP Nexus

SNPshotrs777112652
SNPdbers777112652
MSV3drs777112652
GWAS Ctlgrs777112652
Max Magnitude0
ClinVar
Risk rs777112652(T;T)
Alt rs777112652(T;T)
Reference rs777112652(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene CDC14A
CLNDBN Deafness, autosomal recessive 105
Reversed 0
HGVS NC_000001.10:g.100949885C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000223953.1,