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rs730881082

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881082(A;T)
Make rs730881082(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55151850
GeneTNNI3
is asnp
is mentioned by
dbSNPrs730881082
ebirs730881082
HLIrs730881082
Exacrs730881082
Varsomers730881082
Maprs730881082
PheGenIrs730881082
hapmaprs730881082
1000 genomesrs730881082
hgdprs730881082
ensemblrs730881082
gopubmedrs730881082
geneviewrs730881082
scholarrs730881082
googlers730881082
pharmgkbrs730881082
gwascentralrs730881082
openSNPrs730881082
23andMers730881082
23andMe allrs730881082
SNP Nexus

SNPshotrs730881082
SNPdbers730881082
MSV3drs730881082
GWAS Ctlgrs730881082
Max Magnitude0
ClinVar
Risk rs730881082(T;T)
Alt rs730881082(T;T)
Reference rs730881082(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TNNI3
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.55663218T>A
CLNSRC
CLNACC RCV000159251.1,