Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057517903

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517903(C;C)
Make rs1057517903(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position7575294
GeneDSP
is asnp
is mentioned by
dbSNPrs1057517903
dbSNP (old)rs1057517903
ClinGenrs1057517903
ebirs1057517903
HLIrs1057517903
Exacrs1057517903
Gnomadrs1057517903
Varsomers1057517903
Maprs1057517903
PheGenIrs1057517903
Biobankrs1057517903
1000 genomesrs1057517903
hgdprs1057517903
ensemblrs1057517903
gopubmedrs1057517903
geneviewrs1057517903
scholarrs1057517903
googlers1057517903
pharmgkbrs1057517903
gwascentralrs1057517903
openSNPrs1057517903
23andMers1057517903
23andMe allrs1057517903
SNPshotrs1057517903
SNPdbers1057517903
MSV3drs1057517903
GWAS Ctlgrs1057517903
Max Magnitude0
ClinVar
Risk rs1057517903(C;C)
Alt rs1057517903(C;C)
Reference Rs1057517903(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DSP
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.7575527G>C
CLNSRC
CLNACC RCV000413527.1,