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rs876661405

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661405(A;A)
Make rs876661405(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position44704140
GeneCEACAM16
is asnp
is mentioned by
dbSNPrs876661405
ebirs876661405
HLIrs876661405
Exacrs876661405
Varsomers876661405
Maprs876661405
PheGenIrs876661405
hapmaprs876661405
1000 genomesrs876661405
hgdprs876661405
ensemblrs876661405
gopubmedrs876661405
geneviewrs876661405
scholarrs876661405
googlers876661405
pharmgkbrs876661405
gwascentralrs876661405
openSNPrs876661405
23andMers876661405
23andMe allrs876661405
SNP Nexus

SNPshotrs876661405
SNPdbers876661405
MSV3drs876661405
GWAS Ctlgrs876661405
Max Magnitude0
ClinVar
Risk rs876661405(A;A)
Alt rs876661405(A;A)
Reference rs876661405(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene CEACAM16
CLNDBN Deafness, autosomal dominant 4b
Reversed 0
HGVS NC_000019.9:g.45207410G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000223943.2,