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rs786205543

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205543(A;G)
Make rs786205543(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178685250
GeneTTN
is asnp
is mentioned by
dbSNPrs786205543
ebirs786205543
HLIrs786205543
Exacrs786205543
Varsomers786205543
Maprs786205543
PheGenIrs786205543
hapmaprs786205543
1000 genomesrs786205543
hgdprs786205543
ensemblrs786205543
gopubmedrs786205543
geneviewrs786205543
scholarrs786205543
googlers786205543
pharmgkbrs786205543
gwascentralrs786205543
openSNPrs786205543
23andMers786205543
23andMe allrs786205543
SNP Nexus

SNPshotrs786205543
SNPdbers786205543
MSV3drs786205543
GWAS Ctlgrs786205543
Max Magnitude0
ClinVar
Risk rs786205543(G;G)
Alt rs786205543(G;G)
Reference rs786205543(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179549977T>C
CLNSRC
CLNACC RCV000171321.1,