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rs781540455

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs781540455(C;C)
Make rs781540455(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178575970
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs781540455
ebirs781540455
HLIrs781540455
Exacrs781540455
Varsomers781540455
Maprs781540455
PheGenIrs781540455
hapmaprs781540455
1000 genomesrs781540455
hgdprs781540455
ensemblrs781540455
gopubmedrs781540455
geneviewrs781540455
scholarrs781540455
googlers781540455
pharmgkbrs781540455
gwascentralrs781540455
openSNPrs781540455
23andMers781540455
23andMe allrs781540455
SNP Nexus

SNPshotrs781540455
SNPdbers781540455
MSV3drs781540455
GWAS Ctlgrs781540455
Max Magnitude0
ClinVar
Risk rs781540455(A,C;A,C)
Alt rs781540455(A,C;A,C)
Reference rs781540455(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.179440697G>A
CLNSRC
CLNACC RCV000184256.2,