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rs786205639

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205639(-;-)
Make rs786205639(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178554734
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs786205639
ebirs786205639
HLIrs786205639
Exacrs786205639
Varsomers786205639
Maprs786205639
PheGenIrs786205639
hapmaprs786205639
1000 genomesrs786205639
hgdprs786205639
ensemblrs786205639
gopubmedrs786205639
geneviewrs786205639
scholarrs786205639
googlers786205639
pharmgkbrs786205639
gwascentralrs786205639
openSNPrs786205639
23andMers786205639
23andMe allrs786205639
SNP Nexus

SNPshotrs786205639
SNPdbers786205639
MSV3drs786205639
GWAS Ctlgrs786205639
Max Magnitude0
ClinVar
Risk rs786205639(;)
Alt rs786205639(;)
Reference rs786205639(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179419461delC
CLNSRC
CLNACC RCV000171503.1,