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rs202033121

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs202033121(A;A)
Make rs202033121(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position53938872
GenePCDH15
is asnp
is mentioned by
dbSNPrs202033121
ebirs202033121
HLIrs202033121
Exacrs202033121
Varsomers202033121
Maprs202033121
PheGenIrs202033121
hapmaprs202033121
1000 genomesrs202033121
hgdprs202033121
ensemblrs202033121
gopubmedrs202033121
geneviewrs202033121
scholarrs202033121
googlers202033121
pharmgkbrs202033121
gwascentralrs202033121
openSNPrs202033121
23andMers202033121
23andMe allrs202033121
SNP Nexus

SNPshotrs202033121
SNPdbers202033121
MSV3drs202033121
GWAS Ctlgrs202033121
Max Magnitude0
ClinVar
Risk rs202033121(A;A)
Alt rs202033121(A;A)
Reference rs202033121(G;G)
Significance Other
Disease Usher syndrome
Variation info
Gene PCDH15
CLNDBN Usher syndrome, type 1F
Reversed 0
HGVS NC_000010.10:g.55698632G>A
CLNSRC ClinVar
CLNACC RCV000039723.4,