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rs1057520100

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520100(C;T)
Make rs1057520100(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position62625399
GeneDOCK7
is asnp
is mentioned by
dbSNPrs1057520100
dbSNP (old)rs1057520100
ClinGenrs1057520100
ebirs1057520100
HLIrs1057520100
Exacrs1057520100
Gnomadrs1057520100
Varsomers1057520100
Maprs1057520100
PheGenIrs1057520100
Biobankrs1057520100
1000 genomesrs1057520100
hgdprs1057520100
ensemblrs1057520100
gopubmedrs1057520100
geneviewrs1057520100
scholarrs1057520100
googlers1057520100
pharmgkbrs1057520100
gwascentralrs1057520100
openSNPrs1057520100
23andMers1057520100
23andMe allrs1057520100
SNPshotrs1057520100
SNPdbers1057520100
MSV3drs1057520100
GWAS Ctlgrs1057520100
Max Magnitude0
ClinVar
Risk rs1057520100(T;T)
Alt rs1057520100(T;T)
Reference Rs1057520100(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DOCK7
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.63091070G>A
CLNSRC
CLNACC RCV000433701.1,