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rs754866489

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs754866489(A;A)
Make rs754866489(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178612115
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs754866489
ebirs754866489
HLIrs754866489
Exacrs754866489
Varsomers754866489
Maprs754866489
PheGenIrs754866489
hapmaprs754866489
1000 genomesrs754866489
hgdprs754866489
ensemblrs754866489
gopubmedrs754866489
geneviewrs754866489
scholarrs754866489
googlers754866489
pharmgkbrs754866489
gwascentralrs754866489
openSNPrs754866489
23andMers754866489
23andMe allrs754866489
SNP Nexus

SNPshotrs754866489
SNPdbers754866489
MSV3drs754866489
GWAS Ctlgrs754866489
Max Magnitude0
ClinVar
Risk rs754866489(A;A)
Alt rs754866489(A;A)
Reference rs754866489(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.179476842G>A
CLNSRC
CLNACC RCV000184226.1,