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rs775417975

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs775417975(A;A)
Make rs775417975(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position48487151
GeneFBN1
is asnp
is mentioned by
dbSNPrs775417975
ebirs775417975
HLIrs775417975
Exacrs775417975
Varsomers775417975
Maprs775417975
PheGenIrs775417975
hapmaprs775417975
1000 genomesrs775417975
hgdprs775417975
ensemblrs775417975
gopubmedrs775417975
geneviewrs775417975
scholarrs775417975
googlers775417975
pharmgkbrs775417975
gwascentralrs775417975
openSNPrs775417975
23andMers775417975
23andMe allrs775417975
SNP Nexus

SNPshotrs775417975
SNPdbers775417975
MSV3drs775417975
GWAS Ctlgrs775417975
Max Magnitude0
ClinVar
Risk rs775417975(A;A)
Alt rs775417975(A;A)
Reference rs775417975(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FBN1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.48779348G>T
CLNSRC
CLNACC RCV000181489.2,