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rs587779584

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779584(A;A)
Make rs587779584(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position188996134
GeneCOL3A1, MIR3606
is asnp
is mentioned by
dbSNPrs587779584
ebirs587779584
HLIrs587779584
Exacrs587779584
Varsomers587779584
Maprs587779584
PheGenIrs587779584
hapmaprs587779584
1000 genomesrs587779584
hgdprs587779584
ensemblrs587779584
gopubmedrs587779584
geneviewrs587779584
scholarrs587779584
googlers587779584
pharmgkbrs587779584
gwascentralrs587779584
openSNPrs587779584
23andMers587779584
23andMe allrs587779584
SNP Nexus

SNPshotrs587779584
SNPdbers587779584
MSV3drs587779584
GWAS Ctlgrs587779584
Max Magnitude0
ClinVar
Risk rs587779584(A;A)
Alt rs587779584(A;A)
Reference rs587779584(G;G)
Significance Pathogenic
Disease Ehlers-Danlos syndrome not provided
Variation info
Gene COL3A1 MIR3606
CLNDBN Ehlers-Danlos syndrome, type 4 not provided
Reversed 0
HGVS NC_000002.11:g.189860860G>A
CLNSRC Ehlers-Danlos Syndrome Variant Database COL3A1
CLNACC RCV000087535.1, RCV000181084.2,