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rs766840243

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs766840243(A;A)
Make rs766840243(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178563892
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs766840243
ebirs766840243
HLIrs766840243
Exacrs766840243
Varsomers766840243
Maprs766840243
PheGenIrs766840243
hapmaprs766840243
1000 genomesrs766840243
hgdprs766840243
ensemblrs766840243
gopubmedrs766840243
geneviewrs766840243
scholarrs766840243
googlers766840243
pharmgkbrs766840243
gwascentralrs766840243
openSNPrs766840243
23andMers766840243
23andMe allrs766840243
SNP Nexus

SNPshotrs766840243
SNPdbers766840243
MSV3drs766840243
GWAS Ctlgrs766840243
Max Magnitude0
ClinVar
Risk rs766840243(C;C)
Alt rs766840243(C;C)
Reference rs766840243(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.179428619G>A
CLNSRC
CLNACC RCV000184271.2,