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rs786205602

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205602(G;G)
Make rs786205602(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position137784094
GeneEHMT1
is asnp
is mentioned by
dbSNPrs786205602
ebirs786205602
HLIrs786205602
Exacrs786205602
Varsomers786205602
Maprs786205602
PheGenIrs786205602
hapmaprs786205602
1000 genomesrs786205602
hgdprs786205602
ensemblrs786205602
gopubmedrs786205602
geneviewrs786205602
scholarrs786205602
googlers786205602
pharmgkbrs786205602
gwascentralrs786205602
openSNPrs786205602
23andMers786205602
23andMe allrs786205602
SNP Nexus

SNPshotrs786205602
SNPdbers786205602
MSV3drs786205602
GWAS Ctlgrs786205602
Max Magnitude0
ClinVar
Risk rs786205602(G;G)
Alt rs786205602(G;G)
Reference rs786205602(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC101928897 EHMT1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.140678546T>G
CLNSRC
CLNACC RCV000171431.1,