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rs794728195

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728195(C;T)
Make rs794728195(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48495155
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728195
ebirs794728195
HLIrs794728195
Exacrs794728195
Varsomers794728195
Maprs794728195
PheGenIrs794728195
hapmaprs794728195
1000 genomesrs794728195
hgdprs794728195
ensemblrs794728195
gopubmedrs794728195
geneviewrs794728195
scholarrs794728195
googlers794728195
pharmgkbrs794728195
gwascentralrs794728195
openSNPrs794728195
23andMers794728195
23andMe allrs794728195
SNP Nexus

SNPshotrs794728195
SNPdbers794728195
MSV3drs794728195
GWAS Ctlgrs794728195
Max Magnitude0
ClinVar
Risk rs794728195(T;T)
Alt rs794728195(T;T)
Reference rs794728195(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48787352G>A
CLNSRC
CLNACC RCV000181465.2,