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rs387906700

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906700(A;A)
Make rs387906700(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position77160266
GeneMYO7A
is asnp
is mentioned by
dbSNPrs387906700
ebirs387906700
HLIrs387906700
Exacrs387906700
Varsomers387906700
Maprs387906700
PheGenIrs387906700
hapmaprs387906700
1000 genomesrs387906700
hgdprs387906700
ensemblrs387906700
gopubmedrs387906700
geneviewrs387906700
scholarrs387906700
googlers387906700
pharmgkbrs387906700
gwascentralrs387906700
openSNPrs387906700
23andMers387906700
23andMe allrs387906700
SNP Nexus

SNPshotrs387906700
SNPdbers387906700
MSV3drs387906700
GWAS Ctlgrs387906700
Max Magnitude0
ClinVar
Risk rs387906700(A;A)
Alt rs387906700(A;A)
Reference rs387906700(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO7A
CLNDBN Deafness, autosomal recessive 2
Reversed 0
HGVS NC_000011.9:g.76871312G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022817.23,