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rs746669146

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs746669146(A;A)
Make rs746669146(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178612567
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs746669146
ebirs746669146
HLIrs746669146
Exacrs746669146
Varsomers746669146
Maprs746669146
PheGenIrs746669146
hapmaprs746669146
1000 genomesrs746669146
hgdprs746669146
ensemblrs746669146
gopubmedrs746669146
geneviewrs746669146
scholarrs746669146
googlers746669146
pharmgkbrs746669146
gwascentralrs746669146
openSNPrs746669146
23andMers746669146
23andMe allrs746669146
SNP Nexus

SNPshotrs746669146
SNPdbers746669146
MSV3drs746669146
GWAS Ctlgrs746669146
Max Magnitude0
ClinVar
Risk rs746669146(A,C;A,C)
Alt rs746669146(A,C;A,C)
Reference rs746669146(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.179477294G>C
CLNSRC
CLNACC RCV000184223.2,