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rs373520843

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs373520843(A;A)
Make rs373520843(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position18162639
GeneMYO15A
is asnp
is mentioned by
dbSNPrs373520843
dbSNP (classic)rs373520843
ClinGenrs373520843
ebirs373520843
HLIrs373520843
Exacrs373520843
Gnomadrs373520843
Varsomers373520843
LitVarrs373520843
Maprs373520843
PheGenIrs373520843
Biobankrs373520843
1000 genomesrs373520843
hgdprs373520843
ensemblrs373520843
geneviewrs373520843
scholarrs373520843
googlers373520843
pharmgkbrs373520843
gwascentralrs373520843
openSNPrs373520843
23andMers373520843
SNPshotrs373520843
SNPdbers373520843
MSV3drs373520843
GWAS Ctlgrs373520843
Max Magnitude0
ClinVar
Risk rs373520843(A;A)
Alt rs373520843(A;A)
Reference Rs373520843(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO15A
CLNDBN Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18065953G>A
CLNSRC
CLNACC RCV000454294.1,