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rs797044894

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044894(-;G)
Make rs797044894(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position75028925
GeneKAT6B, LOC105378361
is asnp
is mentioned by
dbSNPrs797044894
ClinGenrs797044894
ebirs797044894
HLIrs797044894
Exacrs797044894
Varsomers797044894
Maprs797044894
PheGenIrs797044894
hapmaprs797044894
1000 genomesrs797044894
hgdprs797044894
ensemblrs797044894
gopubmedrs797044894
geneviewrs797044894
scholarrs797044894
googlers797044894
pharmgkbrs797044894
gwascentralrs797044894
openSNPrs797044894
23andMers797044894
23andMe allrs797044894
SNP Nexus

SNPshotrs797044894
SNPdbers797044894
MSV3drs797044894
GWAS Ctlgrs797044894
Max Magnitude0
ClinVar
Risk rs797044894(G;G)
Alt rs797044894(G;G)
Reference Rs797044894(;)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene KAT6B
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000010.10:g.76788683dupG
CLNSRC
CLNACC RCV000190717.1,