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rs267599036

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267599036(C;T)
Make rs267599036(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178567435
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs267599036
ebirs267599036
HLIrs267599036
Exacrs267599036
Varsomers267599036
Maprs267599036
PheGenIrs267599036
hapmaprs267599036
1000 genomesrs267599036
hgdprs267599036
ensemblrs267599036
gopubmedrs267599036
geneviewrs267599036
scholarrs267599036
googlers267599036
pharmgkbrs267599036
gwascentralrs267599036
openSNPrs267599036
23andMers267599036
23andMe allrs267599036
SNP Nexus

SNPshotrs267599036
SNPdbers267599036
MSV3drs267599036
GWAS Ctlgrs267599036
Max Magnitude0
ClinVar
Risk rs267599036(A,T;A,T)
Alt rs267599036(A,T;A,T)
Reference rs267599036(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.179432162C>A
CLNSRC
CLNACC RCV000184266.2,