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rs786205128

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786205128(-;-)
Make rs786205128(-;G)
Make rs786205128(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position137777891
GeneEHMT1
is asnp
is mentioned by
dbSNPrs786205128
ebirs786205128
HLIrs786205128
Exacrs786205128
Varsomers786205128
Maprs786205128
PheGenIrs786205128
hapmaprs786205128
1000 genomesrs786205128
hgdprs786205128
ensemblrs786205128
gopubmedrs786205128
geneviewrs786205128
scholarrs786205128
googlers786205128
pharmgkbrs786205128
gwascentralrs786205128
openSNPrs786205128
23andMers786205128
23andMe allrs786205128
SNP Nexus

SNPshotrs786205128
SNPdbers786205128
MSV3drs786205128
GWAS Ctlgrs786205128
Max Magnitude0
ClinVar
Risk rs786205128(G;G)
Alt rs786205128(G;G)
Reference rs786205128(;)
Significance Pathogenic
Disease Chromosome 9q deletion syndrome
Variation info
Gene EHMT1
CLNDBN Chromosome 9q deletion syndrome
Reversed 0
HGVS NC_000009.11:g.140672343dupG
CLNSRC
CLNACC RCV000055960.1,