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rs794728238

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728238(C;C)
Make rs794728238(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48446748
GeneFBN1
is asnp
is mentioned by
dbSNPrs794728238
ebirs794728238
HLIrs794728238
Exacrs794728238
Varsomers794728238
Maprs794728238
PheGenIrs794728238
hapmaprs794728238
1000 genomesrs794728238
hgdprs794728238
ensemblrs794728238
gopubmedrs794728238
geneviewrs794728238
scholarrs794728238
googlers794728238
pharmgkbrs794728238
gwascentralrs794728238
openSNPrs794728238
23andMers794728238
23andMe allrs794728238
SNP Nexus

SNPshotrs794728238
SNPdbers794728238
MSV3drs794728238
GWAS Ctlgrs794728238
Max Magnitude0
ClinVar
Risk rs794728238(C;C)
Alt rs794728238(C;C)
Reference rs794728238(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.48738945A>G
CLNSRC
CLNACC RCV000181548.1,