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rs201850378

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201850378(C;T)
Make rs201850378(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position21815724
GeneMIB1
is asnp
is mentioned by
dbSNPrs201850378
ebirs201850378
HLIrs201850378
Exacrs201850378
Varsomers201850378
Maprs201850378
PheGenIrs201850378
hapmaprs201850378
1000 genomesrs201850378
hgdprs201850378
ensemblrs201850378
gopubmedrs201850378
geneviewrs201850378
scholarrs201850378
googlers201850378
pharmgkbrs201850378
gwascentralrs201850378
openSNPrs201850378
23andMers201850378
23andMe allrs201850378
SNP Nexus

SNPshotrs201850378
SNPdbers201850378
MSV3drs201850378
GWAS Ctlgrs201850378
Max Magnitude0
ClinVar
Risk rs201850378(T;T)
Alt rs201850378(T;T)
Reference rs201850378(C;C)
Significance Pathogenic
Disease Left ventricular noncompaction 7
Variation info
Gene MIB1
CLNDBN Left ventricular noncompaction 7
Reversed 0
HGVS NC_000018.9:g.19395685C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000033170.2,