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rs112907302

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs112907302(C;G)
Make rs112907302(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position48420686
GeneFBN1
is asnp
is mentioned by
dbSNPrs112907302
dbSNP (old)rs112907302
ClinGenrs112907302
ebirs112907302
HLIrs112907302
Exacrs112907302
Gnomadrs112907302
Varsomers112907302
Maprs112907302
PheGenIrs112907302
Biobankrs112907302
1000 genomesrs112907302
hgdprs112907302
ensemblrs112907302
gopubmedrs112907302
geneviewrs112907302
scholarrs112907302
googlers112907302
pharmgkbrs112907302
gwascentralrs112907302
openSNPrs112907302
23andMers112907302
23andMe allrs112907302
SNPshotrs112907302
SNPdbers112907302
MSV3drs112907302
GWAS Ctlgrs112907302
Max Magnitude0
ClinVar
Risk rs112907302(G;G)
Alt rs112907302(G;G)
Reference Rs112907302(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.48712883C>T
CLNSRC
CLNACC RCV000493377.1,