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rs111692981

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs111692981(A;A)
Make rs111692981(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position201359257
GeneTNNT2
is asnp
is mentioned by
dbSNPrs111692981
dbSNP (old)rs111692981
ClinGenrs111692981
ebirs111692981
HLIrs111692981
Exacrs111692981
Gnomadrs111692981
Varsomers111692981
Maprs111692981
PheGenIrs111692981
Biobankrs111692981
1000 genomesrs111692981
hgdprs111692981
ensemblrs111692981
gopubmedrs111692981
geneviewrs111692981
scholarrs111692981
googlers111692981
pharmgkbrs111692981
gwascentralrs111692981
openSNPrs111692981
23andMers111692981
23andMe allrs111692981
SNPshotrs111692981
SNPdbers111692981
MSV3drs111692981
GWAS Ctlgrs111692981
Max Magnitude0
ClinVar
Risk rs111692981(A;A) rs111692981(C;C) rs111692981(G;G)
Alt rs111692981(A;A) rs111692981(C;C) rs111692981(G;G)
Reference Rs111692981(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene TNNT2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.201328385T>G
CLNSRC
CLNACC RCV000484808.1,