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rs878853235

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853235(A;G)
Make rs878853235(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position77156889
GeneMYO7A
is asnp
is mentioned by
dbSNPrs878853235
ebirs878853235
HLIrs878853235
Exacrs878853235
Varsomers878853235
Maprs878853235
PheGenIrs878853235
hapmaprs878853235
1000 genomesrs878853235
hgdprs878853235
ensemblrs878853235
gopubmedrs878853235
geneviewrs878853235
scholarrs878853235
googlers878853235
pharmgkbrs878853235
gwascentralrs878853235
openSNPrs878853235
23andMers878853235
23andMe allrs878853235
SNP Nexus

SNPshotrs878853235
SNPdbers878853235
MSV3drs878853235
GWAS Ctlgrs878853235
Max Magnitude0
ClinVar
Risk rs878853235(G;G)
Alt rs878853235(G;G)
Reference rs878853235(A;A)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO7A
CLNDBN Deafness, autosomal recessive 2
Reversed 0
HGVS NC_000011.9:g.76867935A>G
CLNSRC
CLNACC RCV000225019.1,