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rs878853069

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853069(G;G)
Make rs878853069(G;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position150598589
GeneMTM1
is asnp
is mentioned by
dbSNPrs878853069
ebirs878853069
HLIrs878853069
Exacrs878853069
Varsomers878853069
Maprs878853069
PheGenIrs878853069
hapmaprs878853069
1000 genomesrs878853069
hgdprs878853069
ensemblrs878853069
gopubmedrs878853069
geneviewrs878853069
scholarrs878853069
googlers878853069
pharmgkbrs878853069
gwascentralrs878853069
openSNPrs878853069
23andMers878853069
23andMe allrs878853069
SNP Nexus

SNPshotrs878853069
SNPdbers878853069
MSV3drs878853069
GWAS Ctlgrs878853069
Max Magnitude0
ClinVar
Risk rs878853069(G;G)
Alt rs878853069(G;G)
Reference rs878853069(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MTM1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.149767053T>G
CLNSRC
CLNACC RCV000224583.1,