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rs1085307913

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome20
Position44413709
GeneHNF4A
is asnp
is mentioned by
dbSNPrs1085307913
dbSNP (old)rs1085307913
ClinGenrs1085307913
ebirs1085307913
HLIrs1085307913
Exacrs1085307913
Gnomadrs1085307913
Varsomers1085307913
Maprs1085307913
PheGenIrs1085307913
Biobankrs1085307913
1000 genomesrs1085307913
hgdprs1085307913
ensemblrs1085307913
gopubmedrs1085307913
geneviewrs1085307913
scholarrs1085307913
googlers1085307913
pharmgkbrs1085307913
gwascentralrs1085307913
openSNPrs1085307913
23andMers1085307913
23andMe allrs1085307913
SNPshotrs1085307913
SNPdbers1085307913
MSV3drs1085307913
GWAS Ctlgrs1085307913
Max Magnitude0
ClinVar
Risk rs1085307913(A;A)
Alt rs1085307913(A;A)
Reference Rs1085307913(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HNF4A
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.43042349G>A
CLNSRC
CLNACC RCV000489797.1,