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rs72646837

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72646837(G;T)
Make rs72646837(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178594123
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs72646837
ebirs72646837
HLIrs72646837
Exacrs72646837
Varsomers72646837
Maprs72646837
PheGenIrs72646837
hapmaprs72646837
1000 genomesrs72646837
hgdprs72646837
ensemblrs72646837
gopubmedrs72646837
geneviewrs72646837
scholarrs72646837
googlers72646837
pharmgkbrs72646837
gwascentralrs72646837
openSNPrs72646837
23andMers72646837
23andMe allrs72646837
SNP Nexus

SNPshotrs72646837
SNPdbers72646837
MSV3drs72646837
GWAS Ctlgrs72646837
Max Magnitude0
ClinVar
Risk rs72646837(T;T)
Alt rs72646837(T;T)
Reference rs72646837(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179458850C>A
CLNSRC
CLNACC RCV000184244.1,