Have questions? Visit https://www.reddit.com/r/SNPedia

rs529294719

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs529294719(C;T)
Make rs529294719(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position37733611
GeneHNF1B
is asnp
is mentioned by
dbSNPrs529294719
dbSNP (classic)rs529294719
ClinGenrs529294719
ebirs529294719
HLIrs529294719
Exacrs529294719
Gnomadrs529294719
Varsomers529294719
LitVarrs529294719
Maprs529294719
PheGenIrs529294719
Biobankrs529294719
1000 genomesrs529294719
hgdprs529294719
ensemblrs529294719
geneviewrs529294719
scholarrs529294719
googlers529294719
pharmgkbrs529294719
gwascentralrs529294719
openSNPrs529294719
23andMers529294719
23andMe allrs529294719
SNPshotrs529294719
SNPdbers529294719
MSV3drs529294719
GWAS Ctlgrs529294719
Max Magnitude0
ClinVar
Risk rs529294719(G;G) rs529294719(T;T)
Alt rs529294719(G;G) rs529294719(T;T)
Reference Rs529294719(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HNF1B
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.36093604C>G
CLNSRC
CLNACC RCV000479017.1,