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rs886039742

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039742(-;-)
Make rs886039742(-;G)
ReferenceGRCh38.p7 38.3/149
Chromosome10
Position74843114
GeneKAT6B
is asnp
is mentioned by
dbSNPrs886039742
dbSNP (classic)rs886039742
ClinGenrs886039742
ebirs886039742
HLIrs886039742
Exacrs886039742
Gnomadrs886039742
Varsomers886039742
LitVarrs886039742
Maprs886039742
PheGenIrs886039742
Biobankrs886039742
1000 genomesrs886039742
hgdprs886039742
ensemblrs886039742
geneviewrs886039742
scholarrs886039742
googlers886039742
pharmgkbrs886039742
gwascentralrs886039742
openSNPrs886039742
23andMers886039742
SNPshotrs886039742
SNPdbers886039742
MSV3drs886039742
GWAS Ctlgrs886039742
Max Magnitude0
ClinVar
Risk rs886039742(-;-)
Alt rs886039742(-;-)
Reference Rs886039742(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KAT6B
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.76602872delG
CLNSRC
CLNACC RCV000255091.1,