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rs727504285

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504285(C;G)
Make rs727504285(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55151875
GeneTNNI3
is asnp
is mentioned by
dbSNPrs727504285
ebirs727504285
HLIrs727504285
Exacrs727504285
Varsomers727504285
Maprs727504285
PheGenIrs727504285
hapmaprs727504285
1000 genomesrs727504285
hgdprs727504285
ensemblrs727504285
gopubmedrs727504285
geneviewrs727504285
scholarrs727504285
googlers727504285
pharmgkbrs727504285
gwascentralrs727504285
openSNPrs727504285
23andMers727504285
23andMe allrs727504285
SNP Nexus

SNPshotrs727504285
SNPdbers727504285
MSV3drs727504285
GWAS Ctlgrs727504285
Max Magnitude0
ClinVar
Risk rs727504285(G;G)
Alt rs727504285(G;G)
Reference rs727504285(C;C)
Significance Pathogenic
Disease not specified
Variation info
Gene TNNI3
CLNDBN not specified
Reversed 1
HGVS NC_000019.9:g.55663243G>C
CLNSRC
CLNACC RCV000154294.2,