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rs772121356

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs772121356(A;A)
Make rs772121356(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178557730
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs772121356
ebirs772121356
HLIrs772121356
Exacrs772121356
Varsomers772121356
Maprs772121356
PheGenIrs772121356
hapmaprs772121356
1000 genomesrs772121356
hgdprs772121356
ensemblrs772121356
gopubmedrs772121356
geneviewrs772121356
scholarrs772121356
googlers772121356
pharmgkbrs772121356
gwascentralrs772121356
openSNPrs772121356
23andMers772121356
23andMe allrs772121356
SNP Nexus

SNPshotrs772121356
SNPdbers772121356
MSV3drs772121356
GWAS Ctlgrs772121356
Max Magnitude0
ClinVar
Risk rs772121356(A;A)
Alt rs772121356(A;A)
Reference rs772121356(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000002.11:g.179422457G>T
CLNSRC
CLNACC RCV000209702.1,