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rs786205542

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205542(C;G)
Make rs786205542(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178630253
GeneTTN
is asnp
is mentioned by
dbSNPrs786205542
ebirs786205542
HLIrs786205542
Exacrs786205542
Varsomers786205542
Maprs786205542
PheGenIrs786205542
hapmaprs786205542
1000 genomesrs786205542
hgdprs786205542
ensemblrs786205542
gopubmedrs786205542
geneviewrs786205542
scholarrs786205542
googlers786205542
pharmgkbrs786205542
gwascentralrs786205542
openSNPrs786205542
23andMers786205542
23andMe allrs786205542
SNP Nexus

SNPshotrs786205542
SNPdbers786205542
MSV3drs786205542
GWAS Ctlgrs786205542
Max Magnitude0
ClinVar
Risk rs786205542(G;G)
Alt rs786205542(G;G)
Reference rs786205542(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179494980G>C
CLNSRC
CLNACC RCV000171320.1,