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rs111316898

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111316898(C;T)
Make rs111316898(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome20
Position32434579
GeneASXL1
is asnp
is mentioned by
dbSNPrs111316898
dbSNP (old)rs111316898
ClinGenrs111316898
ebirs111316898
HLIrs111316898
Exacrs111316898
Gnomadrs111316898
Varsomers111316898
Maprs111316898
PheGenIrs111316898
Biobankrs111316898
1000 genomesrs111316898
hgdprs111316898
ensemblrs111316898
gopubmedrs111316898
geneviewrs111316898
scholarrs111316898
googlers111316898
pharmgkbrs111316898
gwascentralrs111316898
openSNPrs111316898
23andMers111316898
23andMe allrs111316898
SNPshotrs111316898
SNPdbers111316898
MSV3drs111316898
GWAS Ctlgrs111316898
Max Magnitude0
ClinVar
Risk rs111316898(T;T)
Alt rs111316898(T;T)
Reference Rs111316898(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ASXL1
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.31022382C>T
CLNSRC
CLNACC RCV000331527.1,