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rs1057517261

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TCAA;TCAA) 0 common in clinvar
Make rs1057517261(-;-)
Make rs1057517261(-;TCAA)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position54132959
GenePCDH15
is asnp
is mentioned by
dbSNPrs1057517261
dbSNP (old)rs1057517261
ClinGenrs1057517261
ebirs1057517261
HLIrs1057517261
Exacrs1057517261
Gnomadrs1057517261
Varsomers1057517261
Maprs1057517261
PheGenIrs1057517261
Biobankrs1057517261
1000 genomesrs1057517261
hgdprs1057517261
ensemblrs1057517261
gopubmedrs1057517261
geneviewrs1057517261
scholarrs1057517261
googlers1057517261
pharmgkbrs1057517261
gwascentralrs1057517261
openSNPrs1057517261
23andMers1057517261
23andMe allrs1057517261
SNPshotrs1057517261
SNPdbers1057517261
MSV3drs1057517261
GWAS Ctlgrs1057517261
Max Magnitude0
ClinVar
Risk rs1057517261(-;-)
Alt rs1057517261(-;-)
Reference Rs1057517261(TCAA;TCAA)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene PCDH15
CLNDBN Usher syndrome, type 1F
Reversed 1
HGVS NC_000010.10:g.55892719_55892722delTTGA
CLNSRC
CLNACC RCV000409254.1,