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rs1057524142

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524142(A;A)
Make rs1057524142(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position137800894
GeneEHMT1
is asnp
is mentioned by
dbSNPrs1057524142
dbSNP (classic)rs1057524142
ClinGenrs1057524142
ebirs1057524142
HLIrs1057524142
Exacrs1057524142
Gnomadrs1057524142
Varsomers1057524142
LitVarrs1057524142
Maprs1057524142
PheGenIrs1057524142
Biobankrs1057524142
1000 genomesrs1057524142
hgdprs1057524142
ensemblrs1057524142
geneviewrs1057524142
scholarrs1057524142
googlers1057524142
pharmgkbrs1057524142
gwascentralrs1057524142
openSNPrs1057524142
23andMers1057524142
23andMe allrs1057524142
SNPshotrs1057524142
SNPdbers1057524142
MSV3drs1057524142
GWAS Ctlgrs1057524142
Max Magnitude0
ClinVar
Risk rs1057524142(A;A)
Alt rs1057524142(A;A)
Reference Rs1057524142(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene EHMT1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.140695346G>A
CLNSRC
CLNACC RCV000418911.1,