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rs797045043

From SNPedia

Orientationplus
Make rs797045043(-;-)
Make rs797045043(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position137716931
GeneEHMT1
is asnp
is mentioned by
dbSNPrs797045043
ebirs797045043
HLIrs797045043
Exacrs797045043
Varsomers797045043
Maprs797045043
PheGenIrs797045043
hapmaprs797045043
1000 genomesrs797045043
hgdprs797045043
ensemblrs797045043
gopubmedrs797045043
geneviewrs797045043
scholarrs797045043
googlers797045043
pharmgkbrs797045043
gwascentralrs797045043
openSNPrs797045043
23andMers797045043
23andMe allrs797045043
SNP Nexus

SNPshotrs797045043
SNPdbers797045043
MSV3drs797045043
GWAS Ctlgrs797045043
Max Magnitude
ClinVar
Risk rs797045043(;)
Alt rs797045043(;)
Reference rs797045043(G;G)
Significance Pathogenic
Disease Chromosome 9q deletion syndrome
Variation info
Gene EHMT1
CLNDBN Chromosome 9q deletion syndrome
Reversed 0
HGVS NC_000009.11:g.140611383delG
CLNSRC Baylor College of Medicine
CLNACC RCV000191083.1,