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

rs730881125

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881125(A;A)
Make rs730881125(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201359650
GeneTNNT2
is asnp
is mentioned by
dbSNPrs730881125
ebirs730881125
HLIrs730881125
Exacrs730881125
Varsomers730881125
Maprs730881125
PheGenIrs730881125
hapmaprs730881125
1000 genomesrs730881125
hgdprs730881125
ensemblrs730881125
gopubmedrs730881125
geneviewrs730881125
scholarrs730881125
googlers730881125
pharmgkbrs730881125
gwascentralrs730881125
openSNPrs730881125
23andMers730881125
23andMe allrs730881125
SNP Nexus

SNPshotrs730881125
SNPdbers730881125
MSV3drs730881125
GWAS Ctlgrs730881125
Max Magnitude0
ClinVar
Risk rs730881125(A;A)
Alt rs730881125(A;A)
Reference rs730881125(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNT2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.201328778C>T
CLNSRC
CLNACC RCV000159343.1,