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rs1085307751

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome19
Position35730037
GeneKMT2B
is asnp
is mentioned by
dbSNPrs1085307751
dbSNP (old)rs1085307751
ClinGenrs1085307751
ebirs1085307751
HLIrs1085307751
Exacrs1085307751
Gnomadrs1085307751
Varsomers1085307751
Maprs1085307751
PheGenIrs1085307751
Biobankrs1085307751
1000 genomesrs1085307751
hgdprs1085307751
ensemblrs1085307751
gopubmedrs1085307751
geneviewrs1085307751
scholarrs1085307751
googlers1085307751
pharmgkbrs1085307751
gwascentralrs1085307751
openSNPrs1085307751
23andMers1085307751
23andMe allrs1085307751
SNPshotrs1085307751
SNPdbers1085307751
MSV3drs1085307751
GWAS Ctlgrs1085307751
Max Magnitude0
ClinVar
Risk rs1085307751(C;C)
Alt rs1085307751(C;C)
Reference Rs1085307751(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KMT2B
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.36220938A>C
CLNSRC
CLNACC RCV000489276.1,