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rs727504177

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504177(C;G)
Make rs727504177(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55140947
GeneTNNT1
is asnp
is mentioned by
dbSNPrs727504177
ebirs727504177
HLIrs727504177
Exacrs727504177
Varsomers727504177
Maprs727504177
PheGenIrs727504177
hapmaprs727504177
1000 genomesrs727504177
hgdprs727504177
ensemblrs727504177
gopubmedrs727504177
geneviewrs727504177
scholarrs727504177
googlers727504177
pharmgkbrs727504177
gwascentralrs727504177
openSNPrs727504177
23andMers727504177
23andMe allrs727504177
SNP Nexus

SNPshotrs727504177
SNPdbers727504177
MSV3drs727504177
GWAS Ctlgrs727504177
Max Magnitude0
ClinVar
Risk rs727504177(G;G)
Alt rs727504177(G;G)
Reference rs727504177(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TNNT1
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.55652315G>C
CLNSRC
CLNACC RCV000154009.3,