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rs886041689

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome17
Position37733556
GeneHNF1B
is asnp
is mentioned by
dbSNPrs886041689
dbSNP (classic)rs886041689
ClinGenrs886041689
ebirs886041689
HLIrs886041689
Exacrs886041689
Gnomadrs886041689
Varsomers886041689
LitVarrs886041689
Maprs886041689
PheGenIrs886041689
Biobankrs886041689
1000 genomesrs886041689
hgdprs886041689
ensemblrs886041689
geneviewrs886041689
scholarrs886041689
googlers886041689
pharmgkbrs886041689
gwascentralrs886041689
openSNPrs886041689
23andMers886041689
23andMe allrs886041689
SNPshotrs886041689
SNPdbers886041689
MSV3drs886041689
GWAS Ctlgrs886041689
Max Magnitude0
ClinVar
Risk rs886041689(T;T)
Alt rs886041689(T;T)
Reference Rs886041689(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene HNF1B
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.36093549C>A
CLNSRC
CLNACC RCV000265224.1,