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rs200702600

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200702600(C;T)
Make rs200702600(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position32435795
GeneASXL1
is asnp
is mentioned by
dbSNPrs200702600
ebirs200702600
HLIrs200702600
Exacrs200702600
Varsomers200702600
Maprs200702600
PheGenIrs200702600
hapmaprs200702600
1000 genomesrs200702600
hgdprs200702600
ensemblrs200702600
gopubmedrs200702600
geneviewrs200702600
scholarrs200702600
googlers200702600
pharmgkbrs200702600
gwascentralrs200702600
openSNPrs200702600
23andMers200702600
23andMe allrs200702600
SNP Nexus

SNPshotrs200702600
SNPdbers200702600
MSV3drs200702600
GWAS Ctlgrs200702600
Max Magnitude0
ClinVar
Risk rs200702600(A,T;A,T)
Alt rs200702600(A,T;A,T)
Reference rs200702600(C;C)
Significance Pathogenic
Disease C-like syndrome not specified
Variation info
Gene ASXL1
CLNDBN C-like syndrome not specified
Reversed 0
HGVS NC_000020.10:g.31023598C>A; NC_000020.10:g.31023598C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023978.2, RCV000120095.1,