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rs769488730

From SNPedia

Orientationplus
Geno Mag Summary
(TTTAA;TTTAA) 0 common in clinvar
Make rs769488730(-;-)
Make rs769488730(-;TTTAA)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178547519
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs769488730
ebirs769488730
HLIrs769488730
Exacrs769488730
Varsomers769488730
Maprs769488730
PheGenIrs769488730
hapmaprs769488730
1000 genomesrs769488730
hgdprs769488730
ensemblrs769488730
gopubmedrs769488730
geneviewrs769488730
scholarrs769488730
googlers769488730
pharmgkbrs769488730
gwascentralrs769488730
openSNPrs769488730
23andMers769488730
23andMe allrs769488730
SNP Nexus

SNPshotrs769488730
SNPdbers769488730
MSV3drs769488730
GWAS Ctlgrs769488730
Max Magnitude0
ClinVar
Risk rs769488730(;)
Alt rs769488730(;)
Reference rs769488730(TTTAA;TTTAA)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.179412246_179412250delTTTAA
CLNSRC
CLNACC RCV000184360.1,