Have questions? Visit https://www.reddit.com/r/SNPedia

rs771672410

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs771672410(C;T)
Make rs771672410(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178616485
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs771672410
ebirs771672410
HLIrs771672410
Exacrs771672410
Varsomers771672410
Maprs771672410
PheGenIrs771672410
hapmaprs771672410
1000 genomesrs771672410
hgdprs771672410
ensemblrs771672410
gopubmedrs771672410
geneviewrs771672410
scholarrs771672410
googlers771672410
pharmgkbrs771672410
gwascentralrs771672410
openSNPrs771672410
23andMers771672410
23andMe allrs771672410
SNP Nexus

SNPshotrs771672410
SNPdbers771672410
MSV3drs771672410
GWAS Ctlgrs771672410
Max Magnitude0
ClinVar
Risk rs771672410(T;T)
Alt rs771672410(T;T)
Reference rs771672410(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.179481212C>T
CLNSRC
CLNACC RCV000184219.1,