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rs1044812718

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1044812718(A;A)
Make rs1044812718(A;C)
Make rs1044812718(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position56453154
GeneMIP
is asnp
is mentioned by
dbSNPrs1044812718
dbSNP (old)rs1044812718
ClinGenrs1044812718
ebirs1044812718
HLIrs1044812718
Exacrs1044812718
Gnomadrs1044812718
Varsomers1044812718
Maprs1044812718
PheGenIrs1044812718
Biobankrs1044812718
1000 genomesrs1044812718
hgdprs1044812718
ensemblrs1044812718
gopubmedrs1044812718
geneviewrs1044812718
scholarrs1044812718
googlers1044812718
pharmgkbrs1044812718
gwascentralrs1044812718
openSNPrs1044812718
23andMers1044812718
23andMe allrs1044812718
SNPshotrs1044812718
SNPdbers1044812718
MSV3drs1044812718
GWAS Ctlgrs1044812718
Max Magnitude0
ClinVar
Risk rs1044812718(A;A)
Alt rs1044812718(A;A)
Reference Rs1044812718(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MIP
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.56846938T>G
CLNSRC
CLNACC RCV000430035.1,