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rs730881099

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881099(A;A)
Make rs730881099(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201365253
GeneTNNT2
is asnp
is mentioned by
dbSNPrs730881099
ebirs730881099
HLIrs730881099
Exacrs730881099
Varsomers730881099
Maprs730881099
PheGenIrs730881099
hapmaprs730881099
1000 genomesrs730881099
hgdprs730881099
ensemblrs730881099
gopubmedrs730881099
geneviewrs730881099
scholarrs730881099
googlers730881099
pharmgkbrs730881099
gwascentralrs730881099
openSNPrs730881099
23andMers730881099
23andMe allrs730881099
SNP Nexus

SNPshotrs730881099
SNPdbers730881099
MSV3drs730881099
GWAS Ctlgrs730881099
Max Magnitude0
ClinVar
Risk rs730881099(A,T;A,T)
Alt rs730881099(A,T;A,T)
Reference rs730881099(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TNNT2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.201334381C>A; NC_000001.10:g.201334381C>T
CLNSRC
CLNACC RCV000159287.1, RCV000159286.1,