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rs1057520709

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520709(C;C)
Make rs1057520709(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position53831534
GenePCDH15
is asnp
is mentioned by
dbSNPrs1057520709
dbSNP (old)rs1057520709
ClinGenrs1057520709
ebirs1057520709
HLIrs1057520709
Exacrs1057520709
Gnomadrs1057520709
Varsomers1057520709
Maprs1057520709
PheGenIrs1057520709
Biobankrs1057520709
1000 genomesrs1057520709
hgdprs1057520709
ensemblrs1057520709
gopubmedrs1057520709
geneviewrs1057520709
scholarrs1057520709
googlers1057520709
pharmgkbrs1057520709
gwascentralrs1057520709
openSNPrs1057520709
23andMers1057520709
23andMe allrs1057520709
SNPshotrs1057520709
SNPdbers1057520709
MSV3drs1057520709
GWAS Ctlgrs1057520709
Max Magnitude0
ClinVar
Risk rs1057520709(C;C)
Alt rs1057520709(C;C)
Reference Rs1057520709(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH15
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.55591294C>G
CLNSRC
CLNACC RCV000433340.1,