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rs1057524482

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524482(C;G)
Make rs1057524482(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position28611831
GeneWAC
is asnp
is mentioned by
dbSNPrs1057524482
dbSNP (old)rs1057524482
ClinGenrs1057524482
ebirs1057524482
HLIrs1057524482
Exacrs1057524482
Gnomadrs1057524482
Varsomers1057524482
Maprs1057524482
PheGenIrs1057524482
Biobankrs1057524482
1000 genomesrs1057524482
hgdprs1057524482
ensemblrs1057524482
gopubmedrs1057524482
geneviewrs1057524482
scholarrs1057524482
googlers1057524482
pharmgkbrs1057524482
gwascentralrs1057524482
openSNPrs1057524482
23andMers1057524482
23andMe allrs1057524482
SNPshotrs1057524482
SNPdbers1057524482
MSV3drs1057524482
GWAS Ctlgrs1057524482
Max Magnitude0
ClinVar
Risk rs1057524482(G;G)
Alt rs1057524482(G;G)
Reference Rs1057524482(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene WAC
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.28900760C>G
CLNSRC
CLNACC RCV000444436.1,