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rs398123272

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123272(G;T)
Make rs398123272(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position150663610
GeneMTM1
is asnp
is mentioned by
dbSNPrs398123272
ebirs398123272
HLIrs398123272
Exacrs398123272
Varsomers398123272
Maprs398123272
PheGenIrs398123272
hapmaprs398123272
1000 genomesrs398123272
hgdprs398123272
ensemblrs398123272
gopubmedrs398123272
geneviewrs398123272
scholarrs398123272
googlers398123272
pharmgkbrs398123272
gwascentralrs398123272
openSNPrs398123272
23andMers398123272
23andMe allrs398123272
SNP Nexus

SNPshotrs398123272
SNPdbers398123272
MSV3drs398123272
GWAS Ctlgrs398123272
Max Magnitude0
ClinVar
Risk rs398123272(T;T)
Alt rs398123272(T;T)
Reference rs398123272(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MTM1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.149832083G>T
CLNSRC ClinVar
CLNACC RCV000078434.4,