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rs1057524790

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057524790(C;C)
Make rs1057524790(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position44406234
GeneHNF4A, MIR3646
is asnp
is mentioned by
dbSNPrs1057524790
dbSNP (old)rs1057524790
ClinGenrs1057524790
ebirs1057524790
HLIrs1057524790
Exacrs1057524790
Gnomadrs1057524790
Varsomers1057524790
Maprs1057524790
PheGenIrs1057524790
Biobankrs1057524790
1000 genomesrs1057524790
hgdprs1057524790
ensemblrs1057524790
gopubmedrs1057524790
geneviewrs1057524790
scholarrs1057524790
googlers1057524790
pharmgkbrs1057524790
gwascentralrs1057524790
openSNPrs1057524790
23andMers1057524790
23andMe allrs1057524790
SNPshotrs1057524790
SNPdbers1057524790
MSV3drs1057524790
GWAS Ctlgrs1057524790
Max Magnitude0
ClinVar
Risk rs1057524790(C;C)
Alt rs1057524790(C;C)
Reference Rs1057524790(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MIR3646 HNF4A
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.43034874T>C
CLNSRC
CLNACC RCV000434164.1,