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rs1057517745

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517745(A;A)
Make rs1057517745(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position44406196
GeneHNF4A, MIR3646
is asnp
is mentioned by
dbSNPrs1057517745
dbSNP (old)rs1057517745
ClinGenrs1057517745
ebirs1057517745
HLIrs1057517745
Exacrs1057517745
Gnomadrs1057517745
Varsomers1057517745
LitVarrs1057517745
Maprs1057517745
PheGenIrs1057517745
Biobankrs1057517745
1000 genomesrs1057517745
hgdprs1057517745
ensemblrs1057517745
gopubmedrs1057517745
geneviewrs1057517745
scholarrs1057517745
googlers1057517745
pharmgkbrs1057517745
gwascentralrs1057517745
openSNPrs1057517745
23andMers1057517745
23andMe allrs1057517745
SNPshotrs1057517745
SNPdbers1057517745
MSV3drs1057517745
GWAS Ctlgrs1057517745
Max Magnitude0
ClinVar
Risk rs1057517745(A;A)
Alt rs1057517745(A;A)
Reference Rs1057517745(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MIR3646 HNF4A
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.43034836G>A
CLNSRC
CLNACC RCV000414001.1,