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rs1057520779

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520779(A;A)
Make rs1057520779(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position120993679
GeneHNF1A
is asnp
is mentioned by
dbSNPrs1057520779
dbSNP (old)rs1057520779
ClinGenrs1057520779
ebirs1057520779
HLIrs1057520779
Exacrs1057520779
Gnomadrs1057520779
Varsomers1057520779
Maprs1057520779
PheGenIrs1057520779
Biobankrs1057520779
1000 genomesrs1057520779
hgdprs1057520779
ensemblrs1057520779
gopubmedrs1057520779
geneviewrs1057520779
scholarrs1057520779
googlers1057520779
pharmgkbrs1057520779
gwascentralrs1057520779
openSNPrs1057520779
23andMers1057520779
23andMe allrs1057520779
SNPshotrs1057520779
SNPdbers1057520779
MSV3drs1057520779
GWAS Ctlgrs1057520779
Max Magnitude0
ClinVar
Risk rs1057520779(A;A)
Alt rs1057520779(A;A)
Reference Rs1057520779(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene HNF1A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.121431482G>A
CLNSRC
CLNACC RCV000432234.1,