Have questions? Visit https://www.reddit.com/r/SNPedia

rs781171206

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs781171206(A;A)
Make rs781171206(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178543276
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs781171206
ebirs781171206
HLIrs781171206
Exacrs781171206
Varsomers781171206
Maprs781171206
PheGenIrs781171206
hapmaprs781171206
1000 genomesrs781171206
hgdprs781171206
ensemblrs781171206
gopubmedrs781171206
geneviewrs781171206
scholarrs781171206
googlers781171206
pharmgkbrs781171206
gwascentralrs781171206
openSNPrs781171206
23andMers781171206
23andMe allrs781171206
SNP Nexus

SNPshotrs781171206
SNPdbers781171206
MSV3drs781171206
GWAS Ctlgrs781171206
Max Magnitude0
ClinVar
Risk rs781171206(A;A)
Alt rs781171206(A;A)
Reference rs781171206(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.179408003G>A
CLNSRC
CLNACC RCV000184397.1,