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rs1064795761

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome7
Position152148773
GeneKMT2C
is asnp
is mentioned by
dbSNPrs1064795761
dbSNP (old)rs1064795761
ClinGenrs1064795761
ebirs1064795761
HLIrs1064795761
Exacrs1064795761
Gnomadrs1064795761
Varsomers1064795761
Maprs1064795761
PheGenIrs1064795761
Biobankrs1064795761
1000 genomesrs1064795761
hgdprs1064795761
ensemblrs1064795761
gopubmedrs1064795761
geneviewrs1064795761
scholarrs1064795761
googlers1064795761
pharmgkbrs1064795761
gwascentralrs1064795761
openSNPrs1064795761
23andMers1064795761
23andMe allrs1064795761
SNPshotrs1064795761
SNPdbers1064795761
MSV3drs1064795761
GWAS Ctlgrs1064795761
Max Magnitude0
ClinVar
Risk rs1064795761(T;T)
Alt rs1064795761(T;T)
Reference Rs1064795761(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KMT2C
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.151845858T>A
CLNSRC
CLNACC RCV000485541.1,