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rs587776677

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587776677(-;-)
Make rs587776677(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position23825380
GeneSMARCB1
is asnp
is mentioned by
dbSNPrs587776677
ebirs587776677
HLIrs587776677
Exacrs587776677
Varsomers587776677
Maprs587776677
PheGenIrs587776677
hapmaprs587776677
1000 genomesrs587776677
hgdprs587776677
ensemblrs587776677
gopubmedrs587776677
geneviewrs587776677
scholarrs587776677
googlers587776677
pharmgkbrs587776677
gwascentralrs587776677
openSNPrs587776677
23andMers587776677
23andMe allrs587776677
SNP Nexus

SNPshotrs587776677
SNPdbers587776677
MSV3drs587776677
GWAS Ctlgrs587776677
Max Magnitude0
ClinVar
Risk rs587776677(;)
Alt rs587776677(;)
Reference rs587776677(A;A)
Significance Pathogenic
Disease Malignant rhabdoid tumor
Variation info
Gene SMARCB1
CLNDBN Malignant rhabdoid tumor, somatic
Reversed 0
HGVS NC_000022.10:g.24167567delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000008486.4,