Have questions? Visit https://www.reddit.com/r/SNPedia

rs730881109

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881109(A;G)
Make rs730881109(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201361322
GeneTNNT2
is asnp
is mentioned by
dbSNPrs730881109
ebirs730881109
HLIrs730881109
Exacrs730881109
Varsomers730881109
Maprs730881109
PheGenIrs730881109
hapmaprs730881109
1000 genomesrs730881109
hgdprs730881109
ensemblrs730881109
gopubmedrs730881109
geneviewrs730881109
scholarrs730881109
googlers730881109
pharmgkbrs730881109
gwascentralrs730881109
openSNPrs730881109
23andMers730881109
23andMe allrs730881109
SNP Nexus

SNPshotrs730881109
SNPdbers730881109
MSV3drs730881109
GWAS Ctlgrs730881109
Max Magnitude0
ClinVar
Risk rs730881109(G;G)
Alt rs730881109(G;G)
Reference rs730881109(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNT2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.201330450T>C
CLNSRC
CLNACC RCV000159312.1,