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rs727504268

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504268(A;A)
Make rs727504268(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55151842
GeneTNNI3
is asnp
is mentioned by
dbSNPrs727504268
ebirs727504268
HLIrs727504268
Exacrs727504268
Varsomers727504268
Maprs727504268
PheGenIrs727504268
hapmaprs727504268
1000 genomesrs727504268
hgdprs727504268
ensemblrs727504268
gopubmedrs727504268
geneviewrs727504268
scholarrs727504268
googlers727504268
pharmgkbrs727504268
gwascentralrs727504268
openSNPrs727504268
23andMers727504268
23andMe allrs727504268
SNP Nexus

SNPshotrs727504268
SNPdbers727504268
MSV3drs727504268
GWAS Ctlgrs727504268
Max Magnitude0
ClinVar
Risk rs727504268(A;A)
Alt rs727504268(A;A)
Reference rs727504268(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene TNNI3
CLNDBN not specified
Reversed 1
HGVS NC_000019.9:g.55663210C>T
CLNSRC
CLNACC RCV000154256.2,