Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057518149

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518149(A;A)
Make rs1057518149(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position49039221
GeneKMT2D
is asnp
is mentioned by
dbSNPrs1057518149
dbSNP (old)rs1057518149
ClinGenrs1057518149
ebirs1057518149
HLIrs1057518149
Exacrs1057518149
Gnomadrs1057518149
Varsomers1057518149
Maprs1057518149
PheGenIrs1057518149
Biobankrs1057518149
1000 genomesrs1057518149
hgdprs1057518149
ensemblrs1057518149
gopubmedrs1057518149
geneviewrs1057518149
scholarrs1057518149
googlers1057518149
pharmgkbrs1057518149
gwascentralrs1057518149
openSNPrs1057518149
23andMers1057518149
23andMe allrs1057518149
SNPshotrs1057518149
SNPdbers1057518149
MSV3drs1057518149
GWAS Ctlgrs1057518149
Max Magnitude0
ClinVar
Risk rs1057518149(A;A)
Alt rs1057518149(A;A)
Reference Rs1057518149(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KMT2D
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.49433004C>T
CLNSRC
CLNACC RCV000414121.1,