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rs756715989

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs756715989(C;T)
Make rs756715989(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178580230
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs756715989
ebirs756715989
HLIrs756715989
Exacrs756715989
Varsomers756715989
Maprs756715989
PheGenIrs756715989
hapmaprs756715989
1000 genomesrs756715989
hgdprs756715989
ensemblrs756715989
gopubmedrs756715989
geneviewrs756715989
scholarrs756715989
googlers756715989
pharmgkbrs756715989
gwascentralrs756715989
openSNPrs756715989
23andMers756715989
23andMe allrs756715989
SNP Nexus

SNPshotrs756715989
SNPdbers756715989
MSV3drs756715989
GWAS Ctlgrs756715989
Max Magnitude0
ClinVar
Risk rs756715989(G;G) rs756715989(T;T)
Alt rs756715989(G;G) rs756715989(T;T)
Reference Rs756715989(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.179444957C>G
CLNSRC
CLNACC RCV000184388.1,