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rs78970689

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs78970689(C;G)
Make rs78970689(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48452594
GeneFBN1
is asnp
is mentioned by
dbSNPrs78970689
ebirs78970689
HLIrs78970689
Exacrs78970689
Varsomers78970689
Maprs78970689
PheGenIrs78970689
hapmaprs78970689
1000 genomesrs78970689
hgdprs78970689
ensemblrs78970689
gopubmedrs78970689
geneviewrs78970689
scholarrs78970689
googlers78970689
pharmgkbrs78970689
gwascentralrs78970689
openSNPrs78970689
23andMers78970689
23andMe allrs78970689
SNP Nexus

SNPshotrs78970689
SNPdbers78970689
MSV3drs78970689
GWAS Ctlgrs78970689
Max Magnitude0
ClinVar
Risk rs78970689(G;G)
Alt rs78970689(G;G)
Reference rs78970689(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.48744791C>T
CLNSRC
CLNACC RCV000181546.2,