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rs387906699

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906699(A;A)
Make rs387906699(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position77174831
GeneMYO7A
is asnp
is mentioned by
dbSNPrs387906699
ebirs387906699
HLIrs387906699
Exacrs387906699
Varsomers387906699
Maprs387906699
PheGenIrs387906699
hapmaprs387906699
1000 genomesrs387906699
hgdprs387906699
ensemblrs387906699
gopubmedrs387906699
geneviewrs387906699
scholarrs387906699
googlers387906699
pharmgkbrs387906699
gwascentralrs387906699
openSNPrs387906699
23andMers387906699
23andMe allrs387906699
SNP Nexus

SNPshotrs387906699
SNPdbers387906699
MSV3drs387906699
GWAS Ctlgrs387906699
Max Magnitude0
ClinVar
Risk rs387906699(A;A)
Alt rs387906699(A;A)
Reference rs387906699(G;G)
Significance Pathogenic
Disease Deafness not specified
Variation info
Gene MYO7A
CLNDBN Deafness, autosomal dominant 11 not specified
Reversed 0
HGVS NC_000011.9:g.76885877G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022816.15, RCV000151492.2,