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rs750115837

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs750115837(A;G)
Make rs750115837(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position127826659
GeneENG, LOC105379841
is asnp
is mentioned by
dbSNPrs750115837
dbSNP (classic)rs750115837
ClinGenrs750115837
ebirs750115837
HLIrs750115837
Exacrs750115837
Gnomadrs750115837
Varsomers750115837
LitVarrs750115837
Maprs750115837
PheGenIrs750115837
Biobankrs750115837
1000 genomesrs750115837
hgdprs750115837
ensemblrs750115837
geneviewrs750115837
scholarrs750115837
googlers750115837
pharmgkbrs750115837
gwascentralrs750115837
openSNPrs750115837
23andMers750115837
SNPshotrs750115837
SNPdbers750115837
MSV3drs750115837
GWAS Ctlgrs750115837
Max Magnitude0
ClinVar
Risk rs750115837(G;G)
Alt rs750115837(G;G)
Reference Rs750115837(A;A)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene ENG
CLNDBN not specified not provided
Reversed 0
HGVS NC_000009.11:g.130588938A>G; NC_000009.11:g.130588938A>T
CLNSRC
CLNACC RCV000455548.1, RCV000493483.1,