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rs373145711

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs373145711(C;T)
Make rs373145711(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position32433408
GeneASXL1
is asnp
is mentioned by
dbSNPrs373145711
ebirs373145711
HLIrs373145711
Exacrs373145711
Varsomers373145711
Maprs373145711
PheGenIrs373145711
hapmaprs373145711
1000 genomesrs373145711
hgdprs373145711
ensemblrs373145711
gopubmedrs373145711
geneviewrs373145711
scholarrs373145711
googlers373145711
pharmgkbrs373145711
gwascentralrs373145711
openSNPrs373145711
23andMers373145711
23andMe allrs373145711
SNP Nexus

SNPshotrs373145711
SNPdbers373145711
MSV3drs373145711
GWAS Ctlgrs373145711
Max Magnitude0
ClinVar
Risk rs373145711(T;T)
Alt rs373145711(T;T)
Reference rs373145711(C;C)
Significance Pathogenic
Disease C-like syndrome
Variation info
Gene ASXL1
CLNDBN C-like syndrome
Reversed 0
HGVS NC_000020.10:g.31021211C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023977.2,