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rs1057520678

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520678(A;A)
Make rs1057520678(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position53831482
GenePCDH15
is asnp
is mentioned by
dbSNPrs1057520678
dbSNP (old)rs1057520678
ClinGenrs1057520678
ebirs1057520678
HLIrs1057520678
Exacrs1057520678
Gnomadrs1057520678
Varsomers1057520678
Maprs1057520678
PheGenIrs1057520678
Biobankrs1057520678
1000 genomesrs1057520678
hgdprs1057520678
ensemblrs1057520678
gopubmedrs1057520678
geneviewrs1057520678
scholarrs1057520678
googlers1057520678
pharmgkbrs1057520678
gwascentralrs1057520678
openSNPrs1057520678
23andMers1057520678
23andMe allrs1057520678
SNPshotrs1057520678
SNPdbers1057520678
MSV3drs1057520678
GWAS Ctlgrs1057520678
Max Magnitude0
ClinVar
Risk rs1057520678(A;A)
Alt rs1057520678(A;A)
Reference Rs1057520678(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PCDH15
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.55591242A>T
CLNSRC
CLNACC RCV000435518.1,