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rs886039601

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs886039601(C;G)
Make rs886039601(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome7
Position148810355
GeneEZH2
is asnp
is mentioned by
dbSNPrs886039601
dbSNP (classic)rs886039601
ClinGenrs886039601
ebirs886039601
HLIrs886039601
Exacrs886039601
Gnomadrs886039601
Varsomers886039601
LitVarrs886039601
Maprs886039601
PheGenIrs886039601
Biobankrs886039601
1000 genomesrs886039601
hgdprs886039601
ensemblrs886039601
geneviewrs886039601
scholarrs886039601
googlers886039601
pharmgkbrs886039601
gwascentralrs886039601
openSNPrs886039601
23andMers886039601
23andMe allrs886039601
SNPshotrs886039601
SNPdbers886039601
MSV3drs886039601
GWAS Ctlgrs886039601
Max Magnitude0
ClinVar
Risk rs886039601(G;G)
Alt rs886039601(G;G)
Reference Rs886039601(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EZH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.148507447G>C
CLNSRC
CLNACC RCV000256045.1,