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rs878853108

From SNPedia

Orientationplus
Geno Mag Summary
(TAA;TAA) 0 common in clinvar
Make rs878853108(-;-)
Make rs878853108(-;TAA)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position150641304
GeneMTM1
is asnp
is mentioned by
dbSNPrs878853108
ebirs878853108
HLIrs878853108
Exacrs878853108
Varsomers878853108
Maprs878853108
PheGenIrs878853108
hapmaprs878853108
1000 genomesrs878853108
hgdprs878853108
ensemblrs878853108
gopubmedrs878853108
geneviewrs878853108
scholarrs878853108
googlers878853108
pharmgkbrs878853108
gwascentralrs878853108
openSNPrs878853108
23andMers878853108
23andMe allrs878853108
SNP Nexus

SNPshotrs878853108
SNPdbers878853108
MSV3drs878853108
GWAS Ctlgrs878853108
Max Magnitude0
ClinVar
Risk rs878853108(;)
Alt rs878853108(;)
Reference rs878853108(TAA;TAA)
Significance Pathogenic
Disease not provided
Variation info
Gene MTM1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.149809777_149809779delTAA
CLNSRC
CLNACC RCV000224134.1,