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rs1064795941

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome11
Position44309809
GeneALX4
is asnp
is mentioned by
dbSNPrs1064795941
dbSNP (old)rs1064795941
ClinGenrs1064795941
ebirs1064795941
HLIrs1064795941
Exacrs1064795941
Gnomadrs1064795941
Varsomers1064795941
Maprs1064795941
PheGenIrs1064795941
Biobankrs1064795941
1000 genomesrs1064795941
hgdprs1064795941
ensemblrs1064795941
gopubmedrs1064795941
geneviewrs1064795941
scholarrs1064795941
googlers1064795941
pharmgkbrs1064795941
gwascentralrs1064795941
openSNPrs1064795941
23andMers1064795941
23andMe allrs1064795941
SNPshotrs1064795941
SNPdbers1064795941
MSV3drs1064795941
GWAS Ctlgrs1064795941
Max Magnitude0
ClinVar
Risk rs1064795941(-;-)
Alt rs1064795941(-;-)
Reference Rs1064795941(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALX4
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.44331359delC
CLNSRC
CLNACC RCV000486693.1,