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rs1057523045

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057523045(C;G)
Make rs1057523045(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position7542038
GeneDSP, LOC101928076
is asnp
is mentioned by
dbSNPrs1057523045
dbSNP (old)rs1057523045
ClinGenrs1057523045
ebirs1057523045
HLIrs1057523045
Exacrs1057523045
Gnomadrs1057523045
Varsomers1057523045
Maprs1057523045
PheGenIrs1057523045
Biobankrs1057523045
1000 genomesrs1057523045
hgdprs1057523045
ensemblrs1057523045
gopubmedrs1057523045
geneviewrs1057523045
scholarrs1057523045
googlers1057523045
pharmgkbrs1057523045
gwascentralrs1057523045
openSNPrs1057523045
23andMers1057523045
23andMe allrs1057523045
SNPshotrs1057523045
SNPdbers1057523045
MSV3drs1057523045
GWAS Ctlgrs1057523045
Max Magnitude0
ClinVar
Risk rs1057523045(G;G)
Alt rs1057523045(G;G)
Reference Rs1057523045(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC101928076 DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7542271C>G
CLNSRC
CLNACC RCV000429494.1,