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rs28941777

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs28941777(C;C)
Make rs28941777(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position32392053
GeneWT1
is asnp
is mentioned by
dbSNPrs28941777
ebirs28941777
HLIrs28941777
Exacrs28941777
Varsomers28941777
Maprs28941777
PheGenIrs28941777
hapmaprs28941777
1000 genomesrs28941777
hgdprs28941777
ensemblrs28941777
gopubmedrs28941777
geneviewrs28941777
scholarrs28941777
googlers28941777
pharmgkbrs28941777
gwascentralrs28941777
openSNPrs28941777
23andMers28941777
23andMe allrs28941777
SNP Nexus

SNPshotrs28941777
SNPdbers28941777
MSV3drs28941777
GWAS Ctlgrs28941777
Max Magnitude0
OMIM607102
DescMESANGIAL SCLEROSIS, ISOLATED DIFFUSE
Variant0022
Relatedalso
Neighborrs28941779
Distance27
Neighborrs28942089
Distance619
ClinVar
Risk rs28941777(C;C)
Alt rs28941777(C;C)
Reference rs28941777(T;T)
Significance Pathogenic
Disease Diffuse mesangial sclerosis
Variation info
Gene WT1
CLNDBN Diffuse mesangial sclerosis
Reversed 1
HGVS NC_000011.9:g.32413599A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000003677.2,