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rs878853236

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853236(C;T)
Make rs878853236(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position77174789
GeneMYO7A
is asnp
is mentioned by
dbSNPrs878853236
ebirs878853236
HLIrs878853236
Exacrs878853236
Varsomers878853236
Maprs878853236
PheGenIrs878853236
hapmaprs878853236
1000 genomesrs878853236
hgdprs878853236
ensemblrs878853236
gopubmedrs878853236
geneviewrs878853236
scholarrs878853236
googlers878853236
pharmgkbrs878853236
gwascentralrs878853236
openSNPrs878853236
23andMers878853236
23andMe allrs878853236
SNP Nexus

SNPshotrs878853236
SNPdbers878853236
MSV3drs878853236
GWAS Ctlgrs878853236
Max Magnitude0
ClinVar
Risk rs878853236(T;T)
Alt rs878853236(T;T)
Reference rs878853236(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO7A
CLNDBN Deafness, autosomal recessive 2
Reversed 0
HGVS NC_000011.9:g.76885835C>T
CLNSRC
CLNACC RCV000225048.1,