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rs387907077

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907077(C;T)
Make rs387907077(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position32435485
GeneASXL1
is asnp
is mentioned by
dbSNPrs387907077
ebirs387907077
HLIrs387907077
Exacrs387907077
Varsomers387907077
Maprs387907077
PheGenIrs387907077
hapmaprs387907077
1000 genomesrs387907077
hgdprs387907077
ensemblrs387907077
gopubmedrs387907077
geneviewrs387907077
scholarrs387907077
googlers387907077
pharmgkbrs387907077
gwascentralrs387907077
openSNPrs387907077
23andMers387907077
23andMe allrs387907077
SNP Nexus

SNPshotrs387907077
SNPdbers387907077
MSV3drs387907077
GWAS Ctlgrs387907077
Max Magnitude0
ClinVar
Risk rs387907077(T;T)
Alt rs387907077(T;T)
Reference rs387907077(C;C)
Significance Pathogenic
Disease C-like syndrome
Variation info
Gene ASXL1
CLNDBN C-like syndrome
Reversed 0
HGVS NC_000020.10:g.31023288C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023976.2,