Have questions? Visit https://www.reddit.com/r/SNPedia

rs587779519

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779519(A;A)
Make rs587779519(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position189003410
GeneCOL3A1
is asnp
is mentioned by
dbSNPrs587779519
ebirs587779519
HLIrs587779519
Exacrs587779519
Varsomers587779519
Maprs587779519
PheGenIrs587779519
hapmaprs587779519
1000 genomesrs587779519
hgdprs587779519
ensemblrs587779519
gopubmedrs587779519
geneviewrs587779519
scholarrs587779519
googlers587779519
pharmgkbrs587779519
gwascentralrs587779519
openSNPrs587779519
23andMers587779519
23andMe allrs587779519
SNP Nexus

SNPshotrs587779519
SNPdbers587779519
MSV3drs587779519
GWAS Ctlgrs587779519
Max Magnitude0
ClinVar
Risk rs587779519(A;A)
Alt rs587779519(A;A)
Reference rs587779519(G;G)
Significance Pathogenic
Disease Ehlers-Danlos syndrome
Variation info
Gene COL3A1
CLNDBN Ehlers-Danlos syndrome, type 4
Reversed 0
HGVS NC_000002.11:g.189868136G>A
CLNSRC Ehlers-Danlos Syndrome Variant Database COL3A1
CLNACC RCV000087456.1,