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rs746164064

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs746164064(C;T)
Make rs746164064(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position44705631
GeneCEACAM16
is asnp
is mentioned by
dbSNPrs746164064
ebirs746164064
HLIrs746164064
Exacrs746164064
Varsomers746164064
Maprs746164064
PheGenIrs746164064
hapmaprs746164064
1000 genomesrs746164064
hgdprs746164064
ensemblrs746164064
gopubmedrs746164064
geneviewrs746164064
scholarrs746164064
googlers746164064
pharmgkbrs746164064
gwascentralrs746164064
openSNPrs746164064
23andMers746164064
23andMe allrs746164064
SNP Nexus

SNPshotrs746164064
SNPdbers746164064
MSV3drs746164064
GWAS Ctlgrs746164064
Max Magnitude0
ClinVar
Risk rs746164064(T;T)
Alt rs746164064(T;T)
Reference rs746164064(C;C)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene CEACAM16
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000019.9:g.45208901C>T
CLNSRC
CLNACC RCV000225009.1,