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rs137853001

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853001(C;T)
Make rs137853001(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position54664256
GenePCDH15
is asnp
is mentioned by
dbSNPrs137853001
ebirs137853001
HLIrs137853001
Exacrs137853001
Varsomers137853001
Maprs137853001
PheGenIrs137853001
hapmaprs137853001
1000 genomesrs137853001
hgdprs137853001
ensemblrs137853001
gopubmedrs137853001
geneviewrs137853001
scholarrs137853001
googlers137853001
pharmgkbrs137853001
gwascentralrs137853001
openSNPrs137853001
23andMers137853001
23andMe allrs137853001
SNP Nexus

SNPshotrs137853001
SNPdbers137853001
MSV3drs137853001
GWAS Ctlgrs137853001
Max Magnitude0
OMIM605514
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137853001(T;T)
Alt rs137853001(T;T)
Reference rs137853001(C;C)
Significance Other
Disease Usher syndrome
Variation info
Gene PCDH15
CLNDBN Usher syndrome, type 1F
Reversed 1
HGVS NC_000010.10:g.56424016G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005216.4,