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rs1085307889

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome1
Position201362023
GeneTNNT2
is asnp
is mentioned by
dbSNPrs1085307889
dbSNP (old)rs1085307889
ClinGenrs1085307889
ebirs1085307889
HLIrs1085307889
Exacrs1085307889
Gnomadrs1085307889
Varsomers1085307889
Maprs1085307889
PheGenIrs1085307889
Biobankrs1085307889
1000 genomesrs1085307889
hgdprs1085307889
ensemblrs1085307889
gopubmedrs1085307889
geneviewrs1085307889
scholarrs1085307889
googlers1085307889
pharmgkbrs1085307889
gwascentralrs1085307889
openSNPrs1085307889
23andMers1085307889
23andMe allrs1085307889
SNPshotrs1085307889
SNPdbers1085307889
MSV3drs1085307889
GWAS Ctlgrs1085307889
Max Magnitude0
ClinVar
Risk rs1085307889(A;A)
Alt rs1085307889(A;A)
Reference Rs1085307889(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNT2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.201331151C>T
CLNSRC
CLNACC RCV000490178.1,