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

rs1060505057

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060505057(A;A)
Make rs1060505057(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position31723901
GeneC6orf25, MPIG6B
is asnp
is mentioned by
dbSNPrs1060505057
dbSNP (old)rs1060505057
ClinGenrs1060505057
ebirs1060505057
HLIrs1060505057
Exacrs1060505057
Gnomadrs1060505057
Varsomers1060505057
Maprs1060505057
PheGenIrs1060505057
Biobankrs1060505057
1000 genomesrs1060505057
hgdprs1060505057
ensemblrs1060505057
gopubmedrs1060505057
geneviewrs1060505057
scholarrs1060505057
googlers1060505057
pharmgkbrs1060505057
gwascentralrs1060505057
openSNPrs1060505057
23andMers1060505057
23andMe allrs1060505057
SNPshotrs1060505057
SNPdbers1060505057
MSV3drs1060505057
GWAS Ctlgrs1060505057
Max Magnitude0
ClinVar
Risk rs1060505057(A;A)
Alt rs1060505057(A;A)
Reference Rs1060505057(C;C)
Significance Pathogenic
Disease Thrombocytopenia
Variation info
Gene MPIG6B
CLNDBN Thrombocytopenia, anemia, and myelofibrosis
Reversed 0
HGVS NC_000006.11:g.31691678C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000477970.1,