Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205601

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205601(A;A)
Make rs786205601(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position137717151
GeneEHMT1
is asnp
is mentioned by
dbSNPrs786205601
ebirs786205601
HLIrs786205601
Exacrs786205601
Varsomers786205601
Maprs786205601
PheGenIrs786205601
hapmaprs786205601
1000 genomesrs786205601
hgdprs786205601
ensemblrs786205601
gopubmedrs786205601
geneviewrs786205601
scholarrs786205601
googlers786205601
pharmgkbrs786205601
gwascentralrs786205601
openSNPrs786205601
23andMers786205601
23andMe allrs786205601
SNP Nexus

SNPshotrs786205601
SNPdbers786205601
MSV3drs786205601
GWAS Ctlgrs786205601
Max Magnitude0
ClinVar
Risk rs786205601(A;A)
Alt rs786205601(A;A)
Reference rs786205601(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EHMT1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.140611603G>A
CLNSRC
CLNACC RCV000171430.1,