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rs876657418

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657418(A;A)
Make rs876657418(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position54378943
GenePCDH15
is asnp
is mentioned by
dbSNPrs876657418
ebirs876657418
HLIrs876657418
Exacrs876657418
Varsomers876657418
Maprs876657418
PheGenIrs876657418
hapmaprs876657418
1000 genomesrs876657418
hgdprs876657418
ensemblrs876657418
gopubmedrs876657418
geneviewrs876657418
scholarrs876657418
googlers876657418
pharmgkbrs876657418
gwascentralrs876657418
openSNPrs876657418
23andMers876657418
23andMe allrs876657418
SNP Nexus

SNPshotrs876657418
SNPdbers876657418
MSV3drs876657418
GWAS Ctlgrs876657418
Max Magnitude0
ClinVar
Risk rs876657418(A;A)
Alt rs876657418(A;A)
Reference rs876657418(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene PCDH15
CLNDBN Usher syndrome, type 1
Reversed 1
HGVS NC_000010.10:g.56138703C>T
CLNSRC
CLNACC RCV000222386.1,