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rs559590585

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs559590585(C;T)
Make rs559590585(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178608330
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs559590585
dbSNP (old)rs559590585
ClinGenrs559590585
ebirs559590585
HLIrs559590585
Exacrs559590585
Gnomadrs559590585
Varsomers559590585
Maprs559590585
PheGenIrs559590585
Biobankrs559590585
1000 genomesrs559590585
hgdprs559590585
ensemblrs559590585
gopubmedrs559590585
geneviewrs559590585
scholarrs559590585
googlers559590585
pharmgkbrs559590585
gwascentralrs559590585
openSNPrs559590585
23andMers559590585
23andMe allrs559590585
SNP Nexus

SNPshotrs559590585
SNPdbers559590585
MSV3drs559590585
GWAS Ctlgrs559590585
Max Magnitude0
ClinVar
Risk rs559590585(G;G) rs559590585(T;T)
Alt rs559590585(G;G) rs559590585(T;T)
Reference Rs559590585(C;C)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene TTN TTN-AS1
CLNDBN not provided not specified
Reversed 0
HGVS NC_000002.11:g.179473057C>T
CLNSRC
CLNACC RCV000171319.1, RCV000343935.1,