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rs111033194

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common/normal
(A;C) 3 Carrier of a recessive deafness mutation
Make rs111033194(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position20188912
GeneGJB2
is asnp
is mentioned by
dbSNPrs111033194
dbSNP (classic)rs111033194
ClinGenrs111033194
ebirs111033194
HLIrs111033194
Exacrs111033194
Gnomadrs111033194
Varsomers111033194
LitVarrs111033194
Maprs111033194
PheGenIrs111033194
Biobankrs111033194
1000 genomesrs111033194
hgdprs111033194
ensemblrs111033194
geneviewrs111033194
scholarrs111033194
googlers111033194
pharmgkbrs111033194
gwascentralrs111033194
openSNPrs111033194
23andMers111033194
SNPshotrs111033194
SNPdbers111033194
MSV3drs111033194
GWAS Ctlgrs111033194
Max Magnitude3
ClinVar
Risk rs111033194(C;C)
Alt rs111033194(C;C)
Reference Rs111033194(A;A)
Significance Unknown
Disease not specified
Variation info
Gene GJB2
CLNDBN not specified
Reversed 1
HGVS NC_000013.10:g.20763051T>G
CLNSRC
CLNACC RCV000037870.3,