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rs587776573

From SNPedia

Orientationplus
Stabilizedminus
Geno Mag Summary
(-;TGTCATTTGGTATAAAT) 7.5 Wilms tumor susceptibility (predicted)
(ATTTATACCAAATGACA;ATTTATACCAAATGACA) 0 common in clinvar
(ATTTATACCAAATGACAT;ATTTATACCAAATGACAT) 0 common in clinvar
(TGTCATTTGGTATAAAT;TGTCATTTGGTATAAAT) 0 common in clinvar


Make rs587776573(-;-)
ReferenceGRCh38 38.1/142
Chromosome11
Position32417633
GeneWT1
is asnp
is mentioned by
dbSNPrs587776573
dbSNP (classic)rs587776573
ClinGenrs587776573
ebirs587776573
HLIrs587776573
Exacrs587776573
Gnomadrs587776573
Varsomers587776573
LitVarrs587776573
Maprs587776573
PheGenIrs587776573
Biobankrs587776573
1000 genomesrs587776573
hgdprs587776573
ensemblrs587776573
geneviewrs587776573
scholarrs587776573
googlers587776573
pharmgkbrs587776573
gwascentralrs587776573
openSNPrs587776573
23andMers587776573
23andMe allrs587776573
SNPshotrs587776573
SNPdbers587776573
MSV3drs587776573
GWAS Ctlgrs587776573
Max Magnitude7.5

aka c.242_258del17 (p.Asn81Ilefs)

ClinVar
Risk Rs587776573(TGTCATTTGGTATAAAT;TGTCATTTGGTATAAAT) rs587776573(-;-)
Alt Rs587776573(TGTCATTTGGTATAAAT;TGTCATTTGGTATAAAT) rs587776573(-;-)
Reference Rs587776573(ATTTATACCAAATGACA;ATTTATACCAAATGACA)
Significance Pathogenic
Disease Wilms tumor 1
Variation info
Gene WT1
CLNDBN Wilms tumor 1
Reversed 1
HGVS NC_000011.9:g.32439179_32439195del17
CLNSRC OMIM Allelic Variant
CLNACC RCV000003653.2,