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rs398123268

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CC;CC) 0 common in clinvar
Make rs398123268(-;-)
Make rs398123268(-;CC)
ReferenceGRCh38 38.1/141
ChromosomeX
Position150660374
GeneMTM1
is asnp
is mentioned by
dbSNPrs398123268
ebirs398123268
HLIrs398123268
Exacrs398123268
Varsomers398123268
Maprs398123268
PheGenIrs398123268
hapmaprs398123268
1000 genomesrs398123268
hgdprs398123268
ensemblrs398123268
gopubmedrs398123268
geneviewrs398123268
scholarrs398123268
googlers398123268
pharmgkbrs398123268
gwascentralrs398123268
openSNPrs398123268
23andMers398123268
23andMe allrs398123268
SNP Nexus

SNPshotrs398123268
SNPdbers398123268
MSV3drs398123268
GWAS Ctlgrs398123268
Max Magnitude0
ClinVar
Risk rs398123268(;)
Alt rs398123268(;)
Reference rs398123268(CC;CC)
Significance Pathogenic
Disease not provided
Variation info
Gene MTM1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.149828847_149828848delCC
CLNSRC ClinVar
CLNACC RCV000078430.4,