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rs267606798

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606798(A;A)
Make rs267606798(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position48465825
GeneFBN1
is asnp
is mentioned by
dbSNPrs267606798
ebirs267606798
HLIrs267606798
Exacrs267606798
Varsomers267606798
Maprs267606798
PheGenIrs267606798
hapmaprs267606798
1000 genomesrs267606798
hgdprs267606798
ensemblrs267606798
gopubmedrs267606798
geneviewrs267606798
scholarrs267606798
googlers267606798
pharmgkbrs267606798
gwascentralrs267606798
openSNPrs267606798
23andMers267606798
23andMe allrs267606798
SNP Nexus

SNPshotrs267606798
SNPdbers267606798
MSV3drs267606798
GWAS Ctlgrs267606798
Max Magnitude0
ClinVar
Risk rs267606798(A;A)
Alt rs267606798(A;A)
Reference rs267606798(G;G)
Significance Pathogenic
Disease Stiff skin syndrome Marfan syndrome
Variation info
Gene FBN1
CLNDBN Stiff skin syndrome Marfan syndrome
Reversed 1
HGVS NC_000015.9:g.48758022C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017937.28, RCV000035211.2,