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rs786205129

From SNPedia

Orientationplus
Geno Mag Summary
(TCTT;TCTT) 0 common in clinvar
Make rs786205129(-;-)
Make rs786205129(-;TTCT)
Make rs786205129(TTCT;TTCT)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position137813015
GeneEHMT1
is asnp
is mentioned by
dbSNPrs786205129
ebirs786205129
HLIrs786205129
Exacrs786205129
Varsomers786205129
Maprs786205129
PheGenIrs786205129
hapmaprs786205129
1000 genomesrs786205129
hgdprs786205129
ensemblrs786205129
gopubmedrs786205129
geneviewrs786205129
scholarrs786205129
googlers786205129
pharmgkbrs786205129
gwascentralrs786205129
openSNPrs786205129
23andMers786205129
23andMe allrs786205129
SNP Nexus

SNPshotrs786205129
SNPdbers786205129
MSV3drs786205129
GWAS Ctlgrs786205129
Max Magnitude0
ClinVar
Risk rs786205129(;)
Alt rs786205129(;)
Reference rs786205129(TCTT;TCTT)
Significance Pathogenic
Disease Chromosome 9q deletion syndrome
Variation info
Gene EHMT1
CLNDBN Chromosome 9q deletion syndrome
Reversed 0
HGVS NC_000009.11:g.140707467_140707470delTTCT
CLNSRC
CLNACC RCV000055964.1,