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rs113042313

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs113042313(C;T)
Make rs113042313(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position37710601
GeneHNF1B, LOC105371754
is asnp
is mentioned by
dbSNPrs113042313
dbSNP (old)rs113042313
ClinGenrs113042313
ebirs113042313
HLIrs113042313
Exacrs113042313
Gnomadrs113042313
Varsomers113042313
Maprs113042313
PheGenIrs113042313
Biobankrs113042313
1000 genomesrs113042313
hgdprs113042313
ensemblrs113042313
gopubmedrs113042313
geneviewrs113042313
scholarrs113042313
googlers113042313
pharmgkbrs113042313
gwascentralrs113042313
openSNPrs113042313
23andMers113042313
23andMe allrs113042313
SNPshotrs113042313
SNPdbers113042313
MSV3drs113042313
GWAS Ctlgrs113042313
Max Magnitude0
ClinVar
Risk rs113042313(T;T)
Alt rs113042313(T;T)
Reference Rs113042313(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene HNF1B
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.36070609C>T
CLNSRC
CLNACC RCV000429473.1,