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rs797046064

From SNPedia

Orientationminus
Make rs797046064(-;-)
Make rs797046064(-;TTGT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178634010
GeneTTN
is asnp
is mentioned by
dbSNPrs797046064
ebirs797046064
HLIrs797046064
Exacrs797046064
Varsomers797046064
Maprs797046064
PheGenIrs797046064
hapmaprs797046064
1000 genomesrs797046064
hgdprs797046064
ensemblrs797046064
gopubmedrs797046064
geneviewrs797046064
scholarrs797046064
googlers797046064
pharmgkbrs797046064
gwascentralrs797046064
openSNPrs797046064
23andMers797046064
23andMe allrs797046064
SNP Nexus

SNPshotrs797046064
SNPdbers797046064
MSV3drs797046064
GWAS Ctlgrs797046064
Max Magnitude
ClinVar
Risk rs797046064(;)
Alt rs797046064(;)
Reference rs797046064(TTGT;TTGT)
Significance Pathogenic
Disease Myopathy
Variation info
Gene TTN
CLNDBN Myopathy
Reversed 1
HGVS NC_000002.11:g.179498737_179498740delACAA
CLNSRC
CLNACC RCV000193759.1,