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rs587779602

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779602(A;G)
Make rs587779602(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position188992885
GeneCOL3A1
is asnp
is mentioned by
dbSNPrs587779602
ebirs587779602
HLIrs587779602
Exacrs587779602
Varsomers587779602
Maprs587779602
PheGenIrs587779602
hapmaprs587779602
1000 genomesrs587779602
hgdprs587779602
ensemblrs587779602
gopubmedrs587779602
geneviewrs587779602
scholarrs587779602
googlers587779602
pharmgkbrs587779602
gwascentralrs587779602
openSNPrs587779602
23andMers587779602
23andMe allrs587779602
SNP Nexus

SNPshotrs587779602
SNPdbers587779602
MSV3drs587779602
GWAS Ctlgrs587779602
Max Magnitude0
ClinVar
Risk rs587779602(G;G)
Alt rs587779602(G;G)
Reference rs587779602(A;A)
Significance Pathogenic
Disease Ehlers-Danlos syndrome
Variation info
Gene COL3A1
CLNDBN Ehlers-Danlos syndrome, type 4
Reversed 0
HGVS NC_000002.11:g.189857611A>G
CLNSRC Ehlers-Danlos Syndrome Variant Database COL3A1
CLNACC RCV000087555.1,