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rs387907078

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907078(C;T)
Make rs387907078(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position32434909
GeneASXL1
is asnp
is mentioned by
dbSNPrs387907078
ebirs387907078
HLIrs387907078
Exacrs387907078
Varsomers387907078
Maprs387907078
PheGenIrs387907078
hapmaprs387907078
1000 genomesrs387907078
hgdprs387907078
ensemblrs387907078
gopubmedrs387907078
geneviewrs387907078
scholarrs387907078
googlers387907078
pharmgkbrs387907078
gwascentralrs387907078
openSNPrs387907078
23andMers387907078
23andMe allrs387907078
SNP Nexus

SNPshotrs387907078
SNPdbers387907078
MSV3drs387907078
GWAS Ctlgrs387907078
Max Magnitude0
ClinVar
Risk rs387907078(T;T)
Alt rs387907078(T;T)
Reference rs387907078(C;C)
Significance Pathogenic
Disease C-like syndrome
Variation info
Gene ASXL1
CLNDBN C-like syndrome
Reversed 0
HGVS NC_000020.10:g.31022712C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023980.2,