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rs587779476

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779476(A;A)
Make rs587779476(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position188995056
GeneCOL3A1, MIR3606
is asnp
is mentioned by
dbSNPrs587779476
ebirs587779476
HLIrs587779476
Exacrs587779476
Varsomers587779476
Maprs587779476
PheGenIrs587779476
hapmaprs587779476
1000 genomesrs587779476
hgdprs587779476
ensemblrs587779476
gopubmedrs587779476
geneviewrs587779476
scholarrs587779476
googlers587779476
pharmgkbrs587779476
gwascentralrs587779476
openSNPrs587779476
23andMers587779476
23andMe allrs587779476
SNP Nexus

SNPshotrs587779476
SNPdbers587779476
MSV3drs587779476
GWAS Ctlgrs587779476
Max Magnitude0
ClinVar
Risk rs587779476(A;A)
Alt rs587779476(A;A)
Reference rs587779476(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.189859782G>A
CLNSRC Ehlers-Danlos Syndrome Variant Database COL3A1
CLNACC RCV000087407.1,