Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554310600
rs1554310600
TMEM106B
0.800 GeneticVariation UNIPROT The recurrent mutation in TMEM106B also causes hypomyelinating leukodystrophy in China and is a CpG hotspot. 29444210

2018
dbSNP: rs1554310600
rs1554310600
TMEM106B
A 0.800 GeneticVariation CLINVAR The recurrent mutation in TMEM106B also causes hypomyelinating leukodystrophy in China and is a CpG hotspot. 29444210

2018
dbSNP: rs1554310600
rs1554310600
TMEM106B
0.800 GeneticVariation UNIPROT A recurrent de novo mutation in TMEM106B causes hypomyelinating leukodystrophy. 29186371

2017
dbSNP: rs1554310600
rs1554310600
TMEM106B
A 0.800 GeneticVariation CLINVAR A recurrent de novo mutation in TMEM106B causes hypomyelinating leukodystrophy. 29186371

2017
dbSNP: rs1554310600
rs1554310600
TMEM106B
A 0.800 CausalMutation CLINVAR