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rs1799937

From SNPedia

Orientationminus
Stabilizedminus
Make rs1799937(C;C)
Make rs1799937(C;T)
Make rs1799937(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position32389228
GeneWT1
is asnp
is mentioned by
dbSNPrs1799937
ClinGenrs1799937
ebirs1799937
HLIrs1799937
Exacrs1799937
Varsomers1799937
Maprs1799937
PheGenIrs1799937
hapmaprs1799937
1000 genomesrs1799937
hgdprs1799937
ensemblrs1799937
gopubmedrs1799937
geneviewrs1799937
scholarrs1799937
googlers1799937
pharmgkbrs1799937
gwascentralrs1799937
openSNPrs1799937
23andMers1799937
23andMe allrs1799937
SNP Nexus

SNPshotrs1799937
SNPdbers1799937
MSV3drs1799937
GWAS Ctlgrs1799937
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 26573232OA-icon.png] A genome-wide association study identifies WT1 variant with better response to 5-fluorouracil, pirarubicin and cyclophosphamide neoadjuvant chemotherapy in breast cancer patients


ClinVar
Risk rs1799937(C;C)
Alt rs1799937(C;C)
Reference rs1799937(T;T)
Significance Non-pathogenic
Disease not specified
Variation info
Gene WT1
CLNDBN not specified
Reversed 1
HGVS NC_000011.9:g.32410774A>G
CLNSRC
CLNACC RCV000246241.1,