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rs397514742

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397514742(A;T)
Make rs397514742(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position3412301
GenePRDM16
is asnp
is mentioned by
dbSNPrs397514742
ebirs397514742
HLIrs397514742
Exacrs397514742
Varsomers397514742
Maprs397514742
PheGenIrs397514742
hapmaprs397514742
1000 genomesrs397514742
hgdprs397514742
ensemblrs397514742
gopubmedrs397514742
geneviewrs397514742
scholarrs397514742
googlers397514742
pharmgkbrs397514742
gwascentralrs397514742
openSNPrs397514742
23andMers397514742
23andMe allrs397514742
SNP Nexus

SNPshotrs397514742
SNPdbers397514742
MSV3drs397514742
GWAS Ctlgrs397514742
Max Magnitude0
ClinVar
Risk rs397514742(T;T)
Alt rs397514742(T;T)
Reference rs397514742(A;A)
Significance Pathogenic
Disease Left ventricular noncompaction 8
Variation info
Gene PRDM16
CLNDBN Left ventricular noncompaction 8
Reversed 0
HGVS NC_000001.10:g.3328865A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000054518.2,