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rs727504931

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504931(C;G)
Make rs727504931(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48432915
GeneFBN1
is asnp
is mentioned by
dbSNPrs727504931
ebirs727504931
HLIrs727504931
Exacrs727504931
Varsomers727504931
Maprs727504931
PheGenIrs727504931
hapmaprs727504931
1000 genomesrs727504931
hgdprs727504931
ensemblrs727504931
gopubmedrs727504931
geneviewrs727504931
scholarrs727504931
googlers727504931
pharmgkbrs727504931
gwascentralrs727504931
openSNPrs727504931
23andMers727504931
23andMe allrs727504931
SNP Nexus

SNPshotrs727504931
SNPdbers727504931
MSV3drs727504931
GWAS Ctlgrs727504931
Max Magnitude0
ClinVar
Risk rs727504931(G;G)
Alt rs727504931(G;G)
Reference rs727504931(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene FBN1
CLNDBN not specified
Reversed 1
HGVS NC_000015.9:g.48725112G>C
CLNSRC
CLNACC RCV000156324.1,