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rs150008205

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs150008205(C;T)
Make rs150008205(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201362019
GeneTNNT2
is asnp
is mentioned by
dbSNPrs150008205
ebirs150008205
HLIrs150008205
Exacrs150008205
Varsomers150008205
Maprs150008205
PheGenIrs150008205
hapmaprs150008205
1000 genomesrs150008205
hgdprs150008205
ensemblrs150008205
gopubmedrs150008205
geneviewrs150008205
scholarrs150008205
googlers150008205
pharmgkbrs150008205
gwascentralrs150008205
openSNPrs150008205
23andMers150008205
23andMe allrs150008205
SNP Nexus

SNPshotrs150008205
SNPdbers150008205
MSV3drs150008205
GWAS Ctlgrs150008205
Max Magnitude0
ClinVar
Risk rs150008205(T;T)
Alt rs150008205(T;T)
Reference rs150008205(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNT2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.201331147C>T
CLNSRC
CLNACC RCV000159306.1,