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rs555879

From SNPedia

Orientationminus
Stabilizedminus
Make rs555879(C;C)
Make rs555879(C;T)
Make rs555879(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position49826163
GeneMYO5B
is asnp
is mentioned by
dbSNPrs555879
ClinGenrs555879
ebirs555879
HLIrs555879
Exacrs555879
Varsomers555879
Maprs555879
PheGenIrs555879
hapmaprs555879
1000 genomesrs555879
hgdprs555879
ensemblrs555879
gopubmedrs555879
geneviewrs555879
scholarrs555879
googlers555879
pharmgkbrs555879
gwascentralrs555879
openSNPrs555879
23andMers555879
23andMe allrs555879
SNP Nexus

SNPshotrs555879
SNPdbers555879
MSV3drs555879
GWAS Ctlgrs555879
GMAF0.4715
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 24373531] Genetic risk variants for dyslexia on chromosome 18 in a German cohort
ClinVar
Risk rs555879(T;T)
Alt rs555879(T;T)
Reference rs555879(C;C)
Significance Non-pathogenic
Disease Diarrhea with Microvillus Atrophy
Variation info
Gene MYO5B SNHG22
CLNDBN Diarrhea with Microvillus Atrophy
Reversed 1
HGVS NC_000018.9:g.47352533G>A
CLNSRC
CLNACC RCV000297185.1,