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rs28942088

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
(G;G) 0 common in clinvar
Make rs28942088(C;T)
Make rs28942088(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position102504196
GeneACTR1A, SUFU
is asnp
is mentioned by
dbSNPrs28942088
ebirs28942088
HLIrs28942088
Exacrs28942088
Varsomers28942088
Maprs28942088
PheGenIrs28942088
hapmaprs28942088
1000 genomesrs28942088
hgdprs28942088
ensemblrs28942088
gopubmedrs28942088
geneviewrs28942088
scholarrs28942088
googlers28942088
pharmgkbrs28942088
gwascentralrs28942088
openSNPrs28942088
23andMers28942088
23andMe allrs28942088
SNP Nexus

SNPshotrs28942088
SNPdbers28942088
MSV3drs28942088
GWAS Ctlgrs28942088
Max Magnitude0
NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP
OMIM607035
DescMEDULLOBLASTOMA, SOMATIC
Variant0001
Relatedalso


ClinVar
Risk rs28942088(A;A)
Alt rs28942088(A;A)
Reference rs28942088(G;G)
Significance Pathogenic
Disease Medulloblastoma
Variation info
Gene SUFU ACTR1A
CLNDBN Medulloblastoma
Reversed 1
HGVS NC_000010.10:g.104263953C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003750.4,