Have questions? Visit https://www.reddit.com/r/SNPedia

rs397515566

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397515566(-;-)
Make rs397515566(-;G)
Make rs397515566(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position54369199
GenePCDH15
is asnp
is mentioned by
dbSNPrs397515566
ebirs397515566
HLIrs397515566
Exacrs397515566
Varsomers397515566
Maprs397515566
PheGenIrs397515566
hapmaprs397515566
1000 genomesrs397515566
hgdprs397515566
ensemblrs397515566
gopubmedrs397515566
geneviewrs397515566
scholarrs397515566
googlers397515566
pharmgkbrs397515566
gwascentralrs397515566
openSNPrs397515566
23andMers397515566
23andMe allrs397515566
SNP Nexus

SNPshotrs397515566
SNPdbers397515566
MSV3drs397515566
GWAS Ctlgrs397515566
Max Magnitude0
ClinVar
Risk rs397515566(G;G)
Alt rs397515566(G;G)
Reference rs397515566(;)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene PCDH15
CLNDBN Usher syndrome, type 1G
Reversed 1
HGVS NC_000010.10:g.56128960dupC
CLNSRC ClinVar GeneReviews
CLNACC RCV000055969.1,