Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057517744

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517744(C;T)
Make rs1057517744(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position37739443
GeneHNF1B
is asnp
is mentioned by
dbSNPrs1057517744
dbSNP (old)rs1057517744
ClinGenrs1057517744
ebirs1057517744
HLIrs1057517744
Exacrs1057517744
Gnomadrs1057517744
Varsomers1057517744
Maprs1057517744
PheGenIrs1057517744
Biobankrs1057517744
1000 genomesrs1057517744
hgdprs1057517744
ensemblrs1057517744
gopubmedrs1057517744
geneviewrs1057517744
scholarrs1057517744
googlers1057517744
pharmgkbrs1057517744
gwascentralrs1057517744
openSNPrs1057517744
23andMers1057517744
23andMe allrs1057517744
SNPshotrs1057517744
SNPdbers1057517744
MSV3drs1057517744
GWAS Ctlgrs1057517744
Max Magnitude0
ClinVar
Risk rs1057517744(T;T)
Alt rs1057517744(T;T)
Reference Rs1057517744(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene HNF1B
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.36099434G>A
CLNSRC
CLNACC RCV000413356.1,