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rs587779526

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779526(A;A)
Make rs587779526(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position189003019
GeneCOL3A1
is asnp
is mentioned by
dbSNPrs587779526
ebirs587779526
HLIrs587779526
Exacrs587779526
Varsomers587779526
Maprs587779526
PheGenIrs587779526
hapmaprs587779526
1000 genomesrs587779526
hgdprs587779526
ensemblrs587779526
gopubmedrs587779526
geneviewrs587779526
scholarrs587779526
googlers587779526
pharmgkbrs587779526
gwascentralrs587779526
openSNPrs587779526
23andMers587779526
23andMe allrs587779526
SNP Nexus

SNPshotrs587779526
SNPdbers587779526
MSV3drs587779526
GWAS Ctlgrs587779526
Max Magnitude0
ClinVar
Risk rs587779526(A;A)
Alt rs587779526(A;A)
Reference rs587779526(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.189867745G>A
CLNSRC Ehlers-Danlos Syndrome Variant Database COL3A1
CLNACC RCV000087463.1,