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rs1057518065

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518065(-;-)
Make rs1057518065(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position178624617
GeneTTN
is asnp
is mentioned by
dbSNPrs1057518065
dbSNP (old)rs1057518065
ClinGenrs1057518065
ebirs1057518065
HLIrs1057518065
Exacrs1057518065
Gnomadrs1057518065
Varsomers1057518065
Maprs1057518065
PheGenIrs1057518065
Biobankrs1057518065
1000 genomesrs1057518065
hgdprs1057518065
ensemblrs1057518065
gopubmedrs1057518065
geneviewrs1057518065
scholarrs1057518065
googlers1057518065
pharmgkbrs1057518065
gwascentralrs1057518065
openSNPrs1057518065
23andMers1057518065
23andMe allrs1057518065
SNPshotrs1057518065
SNPdbers1057518065
MSV3drs1057518065
GWAS Ctlgrs1057518065
Max Magnitude0
ClinVar
Risk rs1057518065(-;-)
Alt rs1057518065(-;-)
Reference Rs1057518065(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTN
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.179489344delT
CLNSRC
CLNACC RCV000414635.1,