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rs1057519107

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519107(C;T)
Make rs1057519107(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position31815020
GeneDEPDC5
is asnp
is mentioned by
dbSNPrs1057519107
dbSNP (old)rs1057519107
ClinGenrs1057519107
ebirs1057519107
HLIrs1057519107
Exacrs1057519107
Gnomadrs1057519107
Varsomers1057519107
Maprs1057519107
PheGenIrs1057519107
Biobankrs1057519107
1000 genomesrs1057519107
hgdprs1057519107
ensemblrs1057519107
gopubmedrs1057519107
geneviewrs1057519107
scholarrs1057519107
googlers1057519107
pharmgkbrs1057519107
gwascentralrs1057519107
openSNPrs1057519107
23andMers1057519107
23andMe allrs1057519107
SNPshotrs1057519107
SNPdbers1057519107
MSV3drs1057519107
GWAS Ctlgrs1057519107
Max Magnitude0
ClinVar
Risk rs1057519107(T;T)
Alt rs1057519107(T;T)
Reference Rs1057519107(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DEPDC5
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.32211006C>T
CLNSRC
CLNACC RCV000416201.1,