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rs794728316

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TCA;TCA) 0 common in clinvar
Make rs794728316(-;-)
Make rs794728316(-;TCA)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48437865
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728316
dbSNP (classic)rs794728316
ClinGenrs794728316
ebirs794728316
HLIrs794728316
Exacrs794728316
Gnomadrs794728316
Varsomers794728316
LitVarrs794728316
Maprs794728316
PheGenIrs794728316
Biobankrs794728316
1000 genomesrs794728316
hgdprs794728316
ensemblrs794728316
geneviewrs794728316
scholarrs794728316
googlers794728316
pharmgkbrs794728316
gwascentralrs794728316
openSNPrs794728316
23andMers794728316
SNPshotrs794728316
SNPdbers794728316
MSV3drs794728316
GWAS Ctlgrs794728316
Max Magnitude0
ClinVar
Risk rs794728316(-;-)
Alt rs794728316(-;-)
Reference Rs794728316(TCA;TCA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48730062_48730064delTGA
CLNSRC
CLNACC RCV000181671.2,