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rs200035428

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200035428(G;T)
Make rs200035428(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position21858593
GeneMIB1
is asnp
is mentioned by
dbSNPrs200035428
ebirs200035428
HLIrs200035428
Exacrs200035428
Varsomers200035428
Maprs200035428
PheGenIrs200035428
hapmaprs200035428
1000 genomesrs200035428
hgdprs200035428
ensemblrs200035428
gopubmedrs200035428
geneviewrs200035428
scholarrs200035428
googlers200035428
pharmgkbrs200035428
gwascentralrs200035428
openSNPrs200035428
23andMers200035428
23andMe allrs200035428
SNP Nexus

SNPshotrs200035428
SNPdbers200035428
MSV3drs200035428
GWAS Ctlgrs200035428
Max Magnitude0
ClinVar
Risk rs200035428(T;T)
Alt rs200035428(T;T)
Reference rs200035428(G;G)
Significance Pathogenic
Disease Left ventricular noncompaction 7
Variation info
Gene MIB1
CLNDBN Left ventricular noncompaction 7
Reversed 0
HGVS NC_000018.9:g.19438554G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000033169.2,