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rs141805127

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs141805127(C;T)
Make rs141805127(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201361314
GeneTNNT2
is asnp
is mentioned by
dbSNPrs141805127
ebirs141805127
HLIrs141805127
Exacrs141805127
Varsomers141805127
Maprs141805127
PheGenIrs141805127
hapmaprs141805127
1000 genomesrs141805127
hgdprs141805127
ensemblrs141805127
gopubmedrs141805127
geneviewrs141805127
scholarrs141805127
googlers141805127
pharmgkbrs141805127
gwascentralrs141805127
openSNPrs141805127
23andMers141805127
23andMe allrs141805127
SNP Nexus

SNPshotrs141805127
SNPdbers141805127
MSV3drs141805127
GWAS Ctlgrs141805127
Max Magnitude0
ClinVar
Risk rs141805127(T;T)
Alt rs141805127(T;T)
Reference rs141805127(C;C)
Significance Other
Disease not provided
Variation info
Gene TNNT2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.201330442C>T
CLNSRC
CLNACC RCV000172136.2,