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rs750955319

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs750955319(A;A)
Make rs750955319(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome20
Position32428404
GeneASXL1
is asnp
is mentioned by
dbSNPrs750955319
ebirs750955319
HLIrs750955319
Exacrs750955319
Varsomers750955319
Maprs750955319
PheGenIrs750955319
hapmaprs750955319
1000 genomesrs750955319
hgdprs750955319
ensemblrs750955319
gopubmedrs750955319
geneviewrs750955319
scholarrs750955319
googlers750955319
pharmgkbrs750955319
gwascentralrs750955319
openSNPrs750955319
23andMers750955319
23andMe allrs750955319
SNP Nexus

SNPshotrs750955319
SNPdbers750955319
MSV3drs750955319
GWAS Ctlgrs750955319
Max Magnitude0
ClinVar
Risk rs750955319(A;A)
Alt rs750955319(A;A)
Reference rs750955319(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ASXL1
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.31016207C>A
CLNSRC
CLNACC RCV000171344.1,