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rs757451467

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs757451467(-;-)
Make rs757451467(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178549847
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs757451467
ebirs757451467
HLIrs757451467
Exacrs757451467
Varsomers757451467
Maprs757451467
PheGenIrs757451467
hapmaprs757451467
1000 genomesrs757451467
hgdprs757451467
ensemblrs757451467
gopubmedrs757451467
geneviewrs757451467
scholarrs757451467
googlers757451467
pharmgkbrs757451467
gwascentralrs757451467
openSNPrs757451467
23andMers757451467
23andMe allrs757451467
SNP Nexus

SNPshotrs757451467
SNPdbers757451467
MSV3drs757451467
GWAS Ctlgrs757451467
Max Magnitude0
ClinVar
Risk rs757451467(;)
Alt rs757451467(;)
Reference rs757451467(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.179414574delC
CLNSRC
CLNACC RCV000184358.1,