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rs1057520291

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520291(C;T)
Make rs1057520291(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position120989017
GeneHNF1A
is asnp
is mentioned by
dbSNPrs1057520291
dbSNP (old)rs1057520291
ClinGenrs1057520291
ebirs1057520291
HLIrs1057520291
Exacrs1057520291
Gnomadrs1057520291
Varsomers1057520291
Maprs1057520291
PheGenIrs1057520291
Biobankrs1057520291
1000 genomesrs1057520291
hgdprs1057520291
ensemblrs1057520291
gopubmedrs1057520291
geneviewrs1057520291
scholarrs1057520291
googlers1057520291
pharmgkbrs1057520291
gwascentralrs1057520291
openSNPrs1057520291
23andMers1057520291
23andMe allrs1057520291
SNPshotrs1057520291
SNPdbers1057520291
MSV3drs1057520291
GWAS Ctlgrs1057520291
Max Magnitude0
ClinVar
Risk rs1057520291(T;T)
Alt rs1057520291(T;T)
Reference Rs1057520291(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene HNF1A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.121426820C>T
CLNSRC
CLNACC RCV000436030.1,