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rs1064796972

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome18
Position33744208
GeneASXL3
is asnp
is mentioned by
dbSNPrs1064796972
dbSNP (old)rs1064796972
ClinGenrs1064796972
ebirs1064796972
HLIrs1064796972
Exacrs1064796972
Gnomadrs1064796972
Varsomers1064796972
Maprs1064796972
PheGenIrs1064796972
Biobankrs1064796972
1000 genomesrs1064796972
hgdprs1064796972
ensemblrs1064796972
gopubmedrs1064796972
geneviewrs1064796972
scholarrs1064796972
googlers1064796972
pharmgkbrs1064796972
gwascentralrs1064796972
openSNPrs1064796972
23andMers1064796972
23andMe allrs1064796972
SNPshotrs1064796972
SNPdbers1064796972
MSV3drs1064796972
GWAS Ctlgrs1064796972
Max Magnitude0
ClinVar
Risk rs1064796972(T;T)
Alt rs1064796972(T;T)
Reference Rs1064796972(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ASXL3
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.31324172C>T
CLNSRC
CLNACC RCV000486621.1,