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rs1064796813

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome7
Position152158900
GeneKMT2C
is asnp
is mentioned by
dbSNPrs1064796813
dbSNP (old)rs1064796813
ClinGenrs1064796813
ebirs1064796813
HLIrs1064796813
Exacrs1064796813
Gnomadrs1064796813
Varsomers1064796813
Maprs1064796813
PheGenIrs1064796813
Biobankrs1064796813
1000 genomesrs1064796813
hgdprs1064796813
ensemblrs1064796813
gopubmedrs1064796813
geneviewrs1064796813
scholarrs1064796813
googlers1064796813
pharmgkbrs1064796813
gwascentralrs1064796813
openSNPrs1064796813
23andMers1064796813
23andMe allrs1064796813
SNPshotrs1064796813
SNPdbers1064796813
MSV3drs1064796813
GWAS Ctlgrs1064796813
Max Magnitude0
ClinVar
Risk rs1064796813(G;G)
Alt rs1064796813(G;G)
Reference Rs1064796813(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KMT2C
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.151855985_151855986insC
CLNSRC
CLNACC RCV000478495.1,