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rs886041820

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome17
Position37739577
GeneHNF1B
is asnp
is mentioned by
dbSNPrs886041820
dbSNP (classic)rs886041820
ClinGenrs886041820
ebirs886041820
HLIrs886041820
Exacrs886041820
Gnomadrs886041820
Varsomers886041820
LitVarrs886041820
Maprs886041820
PheGenIrs886041820
Biobankrs886041820
1000 genomesrs886041820
hgdprs886041820
ensemblrs886041820
geneviewrs886041820
scholarrs886041820
googlers886041820
pharmgkbrs886041820
gwascentralrs886041820
openSNPrs886041820
23andMers886041820
23andMe allrs886041820
SNPshotrs886041820
SNPdbers886041820
MSV3drs886041820
GWAS Ctlgrs886041820
Max Magnitude0
ClinVar
Risk rs886041820(C;C)
Alt rs886041820(C;C)
Reference Rs886041820(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene HNF1B
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.36099569dupG
CLNSRC
CLNACC RCV000378370.1,