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rs876657708

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657708(G;T)
Make rs876657708(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position18159680
GeneMYO15A
is asnp
is mentioned by
dbSNPrs876657708
ebirs876657708
HLIrs876657708
Exacrs876657708
Varsomers876657708
Maprs876657708
PheGenIrs876657708
hapmaprs876657708
1000 genomesrs876657708
hgdprs876657708
ensemblrs876657708
gopubmedrs876657708
geneviewrs876657708
scholarrs876657708
googlers876657708
pharmgkbrs876657708
gwascentralrs876657708
openSNPrs876657708
23andMers876657708
23andMe allrs876657708
SNP Nexus

SNPshotrs876657708
SNPdbers876657708
MSV3drs876657708
GWAS Ctlgrs876657708
Max Magnitude0
ClinVar
Risk rs876657708(T;T)
Alt rs876657708(T;T)
Reference rs876657708(G;G)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene MYO15A
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000017.10:g.18062994G>T
CLNSRC
CLNACC RCV000218653.1,