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rs1064793150

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome12
Position120978823
GeneHNF1A
is asnp
is mentioned by
dbSNPrs1064793150
dbSNP (old)rs1064793150
ClinGenrs1064793150
ebirs1064793150
HLIrs1064793150
Exacrs1064793150
Gnomadrs1064793150
Varsomers1064793150
Maprs1064793150
PheGenIrs1064793150
Biobankrs1064793150
1000 genomesrs1064793150
hgdprs1064793150
ensemblrs1064793150
gopubmedrs1064793150
geneviewrs1064793150
scholarrs1064793150
googlers1064793150
pharmgkbrs1064793150
gwascentralrs1064793150
openSNPrs1064793150
23andMers1064793150
23andMe allrs1064793150
SNPshotrs1064793150
SNPdbers1064793150
MSV3drs1064793150
GWAS Ctlgrs1064793150
Max Magnitude0
ClinVar
Risk rs1064793150(G;G)
Alt rs1064793150(G;G)
Reference Rs1064793150(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HNF1A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.121416626T>G
CLNSRC
CLNACC RCV000484372.1,