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rs727504242

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504242(C;T)
Make rs727504242(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55154082
GeneTNNI3
is asnp
is mentioned by
dbSNPrs727504242
ebirs727504242
HLIrs727504242
Exacrs727504242
Varsomers727504242
Maprs727504242
PheGenIrs727504242
hapmaprs727504242
1000 genomesrs727504242
hgdprs727504242
ensemblrs727504242
gopubmedrs727504242
geneviewrs727504242
scholarrs727504242
googlers727504242
pharmgkbrs727504242
gwascentralrs727504242
openSNPrs727504242
23andMers727504242
23andMe allrs727504242
SNP Nexus

SNPshotrs727504242
SNPdbers727504242
MSV3drs727504242
GWAS Ctlgrs727504242
Max Magnitude0
ClinVar
Risk rs727504242(T;T)
Alt rs727504242(T;T)
Reference rs727504242(C;C)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene TNNI3
CLNDBN not specified not provided
Reversed 1
HGVS NC_000019.9:g.55665450G>A
CLNSRC
CLNACC RCV000154210.2, RCV000159230.2,