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rs767837705

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs767837705(G;T)
Make rs767837705(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178542441
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs767837705
ebirs767837705
HLIrs767837705
Exacrs767837705
Varsomers767837705
Maprs767837705
PheGenIrs767837705
hapmaprs767837705
1000 genomesrs767837705
hgdprs767837705
ensemblrs767837705
gopubmedrs767837705
geneviewrs767837705
scholarrs767837705
googlers767837705
pharmgkbrs767837705
gwascentralrs767837705
openSNPrs767837705
23andMers767837705
23andMe allrs767837705
SNP Nexus

SNPshotrs767837705
SNPdbers767837705
MSV3drs767837705
GWAS Ctlgrs767837705
Max Magnitude0
ClinVar
Risk rs767837705(A,T;A,T)
Alt rs767837705(A,T;A,T)
Reference rs767837705(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.179407168G>A
CLNSRC
CLNACC RCV000171309.1,