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rs786205537

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205537(A;A)
Make rs786205537(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178552010
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs786205537
ebirs786205537
HLIrs786205537
Exacrs786205537
Varsomers786205537
Maprs786205537
PheGenIrs786205537
hapmaprs786205537
1000 genomesrs786205537
hgdprs786205537
ensemblrs786205537
gopubmedrs786205537
geneviewrs786205537
scholarrs786205537
googlers786205537
pharmgkbrs786205537
gwascentralrs786205537
openSNPrs786205537
23andMers786205537
23andMe allrs786205537
SNP Nexus

SNPshotrs786205537
SNPdbers786205537
MSV3drs786205537
GWAS Ctlgrs786205537
Max Magnitude0
ClinVar
Risk rs786205537(A;A)
Alt rs786205537(A;A)
Reference rs786205537(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179416737A>T
CLNSRC
CLNACC RCV000171311.1,