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rs368979510

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs368979510(A;A)
Make rs368979510(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48463209
GeneFBN1
is asnp
is mentioned by
dbSNPrs368979510
dbSNP (old)rs368979510
ClinGenrs368979510
ebirs368979510
HLIrs368979510
Exacrs368979510
Gnomadrs368979510
Varsomers368979510
Maprs368979510
PheGenIrs368979510
Biobankrs368979510
1000 genomesrs368979510
hgdprs368979510
ensemblrs368979510
gopubmedrs368979510
geneviewrs368979510
scholarrs368979510
googlers368979510
pharmgkbrs368979510
gwascentralrs368979510
openSNPrs368979510
23andMers368979510
23andMe allrs368979510
SNP Nexus

SNPshotrs368979510
SNPdbers368979510
MSV3drs368979510
GWAS Ctlgrs368979510
Max Magnitude0
ClinVar
Risk rs368979510(A;A) rs368979510(C;C)
Alt rs368979510(A;A) rs368979510(C;C)
Reference Rs368979510(G;G)
Significance Other
Disease not specified not provided
Variation info
Gene FBN1
CLNDBN not specified not provided
Reversed 0
HGVS NC_000015.9:g.48755406G>A; NC_000015.9:g.48755406G>C
CLNSRC
CLNACC RCV000241566.2, RCV000181538.1,