Have questions? Visit https://www.reddit.com/r/SNPedia

rs1064793759

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Chromosome7
Position152183135
GeneKMT2C
is asnp
is mentioned by
dbSNPrs1064793759
dbSNP (classic)rs1064793759
ClinGenrs1064793759
ebirs1064793759
HLIrs1064793759
Exacrs1064793759
Gnomadrs1064793759
Varsomers1064793759
LitVarrs1064793759
Maprs1064793759
PheGenIrs1064793759
Biobankrs1064793759
1000 genomesrs1064793759
hgdprs1064793759
ensemblrs1064793759
geneviewrs1064793759
scholarrs1064793759
googlers1064793759
pharmgkbrs1064793759
gwascentralrs1064793759
openSNPrs1064793759
23andMers1064793759
23andMe allrs1064793759
SNPshotrs1064793759
SNPdbers1064793759
MSV3drs1064793759
GWAS Ctlgrs1064793759
Max Magnitude0
ClinVar
Risk rs1064793759(-;-)
Alt rs1064793759(-;-)
Reference Rs1064793759(AG;AG)
Significance Pathogenic
Disease not provided
Variation info
Gene KMT2C
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.151880220_151880221delCT
CLNSRC
CLNACC RCV000479700.1,