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rs878853237

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853237(C;C)
Make rs878853237(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position77142719
GeneMYO7A
is asnp
is mentioned by
dbSNPrs878853237
ebirs878853237
HLIrs878853237
Exacrs878853237
Varsomers878853237
Maprs878853237
PheGenIrs878853237
hapmaprs878853237
1000 genomesrs878853237
hgdprs878853237
ensemblrs878853237
gopubmedrs878853237
geneviewrs878853237
scholarrs878853237
googlers878853237
pharmgkbrs878853237
gwascentralrs878853237
openSNPrs878853237
23andMers878853237
23andMe allrs878853237
SNP Nexus

SNPshotrs878853237
SNPdbers878853237
MSV3drs878853237
GWAS Ctlgrs878853237
Max Magnitude0
ClinVar
Risk rs878853237(C;C)
Alt rs878853237(C;C)
Reference rs878853237(T;T)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO7A
CLNDBN Deafness, autosomal recessive 2
Reversed 0
HGVS NC_000011.9:g.76853765T>C
CLNSRC
CLNACC RCV000225048.1,