Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057517150

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs1057517150(-;-)
Make rs1057517150(-;TC)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position54153113
GenePCDH15
is asnp
is mentioned by
dbSNPrs1057517150
dbSNP (old)rs1057517150
ClinGenrs1057517150
ebirs1057517150
HLIrs1057517150
Exacrs1057517150
Gnomadrs1057517150
Varsomers1057517150
Maprs1057517150
PheGenIrs1057517150
Biobankrs1057517150
1000 genomesrs1057517150
hgdprs1057517150
ensemblrs1057517150
gopubmedrs1057517150
geneviewrs1057517150
scholarrs1057517150
googlers1057517150
pharmgkbrs1057517150
gwascentralrs1057517150
openSNPrs1057517150
23andMers1057517150
23andMe allrs1057517150
SNPshotrs1057517150
SNPdbers1057517150
MSV3drs1057517150
GWAS Ctlgrs1057517150
Max Magnitude0
ClinVar
Risk rs1057517150(-;-)
Alt rs1057517150(-;-)
Reference Rs1057517150(TC;TC)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene PCDH15
CLNDBN Usher syndrome, type 1F
Reversed 1
HGVS NC_000010.10:g.55912873_55912874delGA
CLNSRC
CLNACC RCV000411988.1,