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rs794729370

From SNPedia

Orientationminus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs794729370(-;-)
Make rs794729370(-;CA)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178773945
GeneTTN
is asnp
is mentioned by
dbSNPrs794729370
ebirs794729370
HLIrs794729370
Exacrs794729370
Varsomers794729370
Maprs794729370
PheGenIrs794729370
hapmaprs794729370
1000 genomesrs794729370
hgdprs794729370
ensemblrs794729370
gopubmedrs794729370
geneviewrs794729370
scholarrs794729370
googlers794729370
pharmgkbrs794729370
gwascentralrs794729370
openSNPrs794729370
23andMers794729370
23andMe allrs794729370
SNP Nexus

SNPshotrs794729370
SNPdbers794729370
MSV3drs794729370
GWAS Ctlgrs794729370
Max Magnitude0
ClinVar
Risk rs794729370(;)
Alt rs794729370(;)
Reference rs794729370(CA;CA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179638672_179638673delTG
CLNSRC
CLNACC RCV000184371.1,