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rs869312881

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312881(A;A)
Make rs869312881(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position201365286
GeneTNNT2
is asnp
is mentioned by
dbSNPrs869312881
ebirs869312881
HLIrs869312881
Exacrs869312881
Varsomers869312881
Maprs869312881
PheGenIrs869312881
hapmaprs869312881
1000 genomesrs869312881
hgdprs869312881
ensemblrs869312881
gopubmedrs869312881
geneviewrs869312881
scholarrs869312881
googlers869312881
pharmgkbrs869312881
gwascentralrs869312881
openSNPrs869312881
23andMers869312881
23andMe allrs869312881
SNP Nexus

SNPshotrs869312881
SNPdbers869312881
MSV3drs869312881
GWAS Ctlgrs869312881
Max Magnitude0
ClinVar
Risk rs869312881(A;A)
Alt rs869312881(A;A)
Reference rs869312881(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.201334414C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000210349.1,