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rs587779621

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779621(A;A)
Make rs587779621(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position188994734
GeneCOL3A1, MIR3606
is asnp
is mentioned by
dbSNPrs587779621
ebirs587779621
HLIrs587779621
Exacrs587779621
Varsomers587779621
Maprs587779621
PheGenIrs587779621
hapmaprs587779621
1000 genomesrs587779621
hgdprs587779621
ensemblrs587779621
gopubmedrs587779621
geneviewrs587779621
scholarrs587779621
googlers587779621
pharmgkbrs587779621
gwascentralrs587779621
openSNPrs587779621
23andMers587779621
23andMe allrs587779621
SNP Nexus

SNPshotrs587779621
SNPdbers587779621
MSV3drs587779621
GWAS Ctlgrs587779621
Max Magnitude0
ClinVar
Risk rs587779621(A;A)
Alt rs587779621(A;A)
Reference rs587779621(G;G)
Significance Pathogenic
Disease Ehlers-Danlos syndrome
Variation info
Gene COL3A1 MIR3606
CLNDBN Ehlers-Danlos syndrome, type 4
Reversed 0
HGVS NC_000002.11:g.189859460G>A
CLNSRC Ehlers-Danlos Syndrome Variant Database COL3A1
CLNACC RCV000087581.1,