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rs2555818

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2555818(A;G)
Make rs2555818(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position178546299
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs2555818
dbSNP (classic)rs2555818
ClinGenrs2555818
ebirs2555818
HLIrs2555818
Exacrs2555818
Gnomadrs2555818
Varsomers2555818
LitVarrs2555818
Maprs2555818
PheGenIrs2555818
Biobankrs2555818
1000 genomesrs2555818
hgdprs2555818
ensemblrs2555818
geneviewrs2555818
scholarrs2555818
googlers2555818
pharmgkbrs2555818
gwascentralrs2555818
openSNPrs2555818
23andMers2555818
23andMe allrs2555818
SNPshotrs2555818
SNPdbers2555818
MSV3drs2555818
GWAS Ctlgrs2555818
Max Magnitude0
? (A;A) (A;G) (G;G) 28
ClinVar
Risk rs2555818(C;C) rs2555818(G;G)
Alt rs2555818(C;C) rs2555818(G;G)
Reference Rs2555818(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.179411026A>C
CLNSRC
CLNACC RCV000485162.1,