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rs786205552

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205552(C;C)
Make rs786205552(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome20
Position32435701
GeneASXL1
is asnp
is mentioned by
dbSNPrs786205552
ebirs786205552
HLIrs786205552
Exacrs786205552
Varsomers786205552
Maprs786205552
PheGenIrs786205552
hapmaprs786205552
1000 genomesrs786205552
hgdprs786205552
ensemblrs786205552
gopubmedrs786205552
geneviewrs786205552
scholarrs786205552
googlers786205552
pharmgkbrs786205552
gwascentralrs786205552
openSNPrs786205552
23andMers786205552
23andMe allrs786205552
SNP Nexus

SNPshotrs786205552
SNPdbers786205552
MSV3drs786205552
GWAS Ctlgrs786205552
Max Magnitude0
ClinVar
Risk rs786205552(C;C)
Alt rs786205552(C;C)
Reference rs786205552(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ASXL1
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.31023504G>C
CLNSRC
CLNACC RCV000171345.1,