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rs587783644

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783644(C;C)
Make rs587783644(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position20189475
GeneGJB2
is asnp
is mentioned by
dbSNPrs587783644
ebirs587783644
HLIrs587783644
Exacrs587783644
Varsomers587783644
Maprs587783644
PheGenIrs587783644
hapmaprs587783644
1000 genomesrs587783644
hgdprs587783644
ensemblrs587783644
gopubmedrs587783644
geneviewrs587783644
scholarrs587783644
googlers587783644
pharmgkbrs587783644
gwascentralrs587783644
openSNPrs587783644
23andMers587783644
23andMe allrs587783644
SNP Nexus

SNPshotrs587783644
SNPdbers587783644
MSV3drs587783644
GWAS Ctlgrs587783644
Max Magnitude0
ClinVar
Risk rs587783644(C;C)
Alt rs587783644(C;C)
Reference rs587783644(T;T)
Significance Pathogenic
Disease Hearing impairment
Variation info
Gene GJB2
CLNDBN Hearing impairment
Reversed 1
HGVS NC_000013.10:g.20763614A>G
CLNSRC
CLNACC RCV000146004.1,