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rs765512476

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs765512476(C;T)
Make rs765512476(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178571292
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs765512476
ebirs765512476
HLIrs765512476
Exacrs765512476
Varsomers765512476
Maprs765512476
PheGenIrs765512476
hapmaprs765512476
1000 genomesrs765512476
hgdprs765512476
ensemblrs765512476
gopubmedrs765512476
geneviewrs765512476
scholarrs765512476
googlers765512476
pharmgkbrs765512476
gwascentralrs765512476
openSNPrs765512476
23andMers765512476
23andMe allrs765512476
SNP Nexus

SNPshotrs765512476
SNPdbers765512476
MSV3drs765512476
GWAS Ctlgrs765512476
Max Magnitude0
ClinVar
Risk rs765512476(T;T)
Alt rs765512476(T;T)
Reference rs765512476(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.179436019C>T
CLNSRC
CLNACC RCV000171314.1,