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rs121964861

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964861(A;A)
Make rs121964861(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position201359636
GeneTNNT2
is asnp
is mentioned by
dbSNPrs121964861
ebirs121964861
HLIrs121964861
Exacrs121964861
Varsomers121964861
Maprs121964861
PheGenIrs121964861
hapmaprs121964861
1000 genomesrs121964861
hgdprs121964861
ensemblrs121964861
gopubmedrs121964861
geneviewrs121964861
scholarrs121964861
googlers121964861
pharmgkbrs121964861
gwascentralrs121964861
openSNPrs121964861
23andMers121964861
23andMe allrs121964861
SNP Nexus

SNPshotrs121964861
SNPdbers121964861
MSV3drs121964861
GWAS Ctlgrs121964861
Max Magnitude0
OMIM191045
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121964861(A,T;A,T)
Alt rs121964861(A,T;A,T)
Reference rs121964861(G;G)
Significance Pathogenic
Disease Left ventricular noncompaction 6
Variation info
Gene TNNT2
CLNDBN Left ventricular noncompaction 6
Reversed 1
HGVS NC_000001.10:g.201328764C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013229.22,