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rs1057524479

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524479(C;T)
Make rs1057524479(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position37699168
GeneHNF1B
is asnp
is mentioned by
dbSNPrs1057524479
dbSNP (old)rs1057524479
ClinGenrs1057524479
ebirs1057524479
HLIrs1057524479
Exacrs1057524479
Gnomadrs1057524479
Varsomers1057524479
Maprs1057524479
PheGenIrs1057524479
Biobankrs1057524479
1000 genomesrs1057524479
hgdprs1057524479
ensemblrs1057524479
gopubmedrs1057524479
geneviewrs1057524479
scholarrs1057524479
googlers1057524479
pharmgkbrs1057524479
gwascentralrs1057524479
openSNPrs1057524479
23andMers1057524479
23andMe allrs1057524479
SNPshotrs1057524479
SNPdbers1057524479
MSV3drs1057524479
GWAS Ctlgrs1057524479
Max Magnitude0
ClinVar
Risk rs1057524479(T;T)
Alt rs1057524479(T;T)
Reference Rs1057524479(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HNF1B
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.36059174G>A
CLNSRC
CLNACC RCV000429830.1,