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

rs1057521851

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521851(A;C)
Make rs1057521851(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position90401312
GeneCALM1
is asnp
is mentioned by
dbSNPrs1057521851
dbSNP (old)rs1057521851
ClinGenrs1057521851
ebirs1057521851
HLIrs1057521851
Exacrs1057521851
Gnomadrs1057521851
Varsomers1057521851
Maprs1057521851
PheGenIrs1057521851
Biobankrs1057521851
1000 genomesrs1057521851
hgdprs1057521851
ensemblrs1057521851
gopubmedrs1057521851
geneviewrs1057521851
scholarrs1057521851
googlers1057521851
pharmgkbrs1057521851
gwascentralrs1057521851
openSNPrs1057521851
23andMers1057521851
23andMe allrs1057521851
SNPshotrs1057521851
SNPdbers1057521851
MSV3drs1057521851
GWAS Ctlgrs1057521851
Max Magnitude0
ClinVar
Risk rs1057521851(C;C)
Alt rs1057521851(C;C)
Reference Rs1057521851(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CALM1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.90867656A>C
CLNSRC
CLNACC RCV000431318.1,