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rs199625633

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199625633(C;T)
Make rs199625633(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position48497371
GeneFBN1
is asnp
is mentioned by
dbSNPrs199625633
ebirs199625633
HLIrs199625633
Exacrs199625633
Varsomers199625633
Maprs199625633
PheGenIrs199625633
hapmaprs199625633
1000 genomesrs199625633
hgdprs199625633
ensemblrs199625633
gopubmedrs199625633
geneviewrs199625633
scholarrs199625633
googlers199625633
pharmgkbrs199625633
gwascentralrs199625633
openSNPrs199625633
23andMers199625633
23andMe allrs199625633
SNP Nexus

SNPshotrs199625633
SNPdbers199625633
MSV3drs199625633
GWAS Ctlgrs199625633
Max Magnitude0
ClinVar
Risk rs199625633(T;T)
Alt rs199625633(T;T)
Reference rs199625633(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene FBN1
CLNDBN not specified
Reversed 0
HGVS NC_000015.9:g.48789568C>T
CLNSRC ClinVar
CLNACC RCV000035133.3,