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rs730881101

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881101(A;A)
Make rs730881101(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201364335
GeneTNNT2
is asnp
is mentioned by
dbSNPrs730881101
ebirs730881101
HLIrs730881101
Exacrs730881101
Varsomers730881101
Maprs730881101
PheGenIrs730881101
hapmaprs730881101
1000 genomesrs730881101
hgdprs730881101
ensemblrs730881101
gopubmedrs730881101
geneviewrs730881101
scholarrs730881101
googlers730881101
pharmgkbrs730881101
gwascentralrs730881101
openSNPrs730881101
23andMers730881101
23andMe allrs730881101
SNP Nexus

SNPshotrs730881101
SNPdbers730881101
MSV3drs730881101
GWAS Ctlgrs730881101
Max Magnitude0
ClinVar
Risk rs730881101(A;A)
Alt rs730881101(A;A)
Reference rs730881101(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TNNT2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.201333463C>T
CLNSRC
CLNACC RCV000159297.1,