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rs876657707

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876657707(-;-)
Make rs876657707(-;C)
Make rs876657707(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position18119985
GeneMYO15A
is asnp
is mentioned by
dbSNPrs876657707
ebirs876657707
HLIrs876657707
Exacrs876657707
Varsomers876657707
Maprs876657707
PheGenIrs876657707
hapmaprs876657707
1000 genomesrs876657707
hgdprs876657707
ensemblrs876657707
gopubmedrs876657707
geneviewrs876657707
scholarrs876657707
googlers876657707
pharmgkbrs876657707
gwascentralrs876657707
openSNPrs876657707
23andMers876657707
23andMe allrs876657707
SNP Nexus

SNPshotrs876657707
SNPdbers876657707
MSV3drs876657707
GWAS Ctlgrs876657707
Max Magnitude0
ClinVar
Risk rs876657707(C;C)
Alt rs876657707(C;C)
Reference rs876657707(;)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene MYO15A
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000017.10:g.18023299dupC
CLNSRC
CLNACC RCV000223213.1,