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rs587779693

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779693(A;A)
Make rs587779693(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position188995738
GeneCOL3A1, MIR3606
is asnp
is mentioned by
dbSNPrs587779693
ebirs587779693
HLIrs587779693
Exacrs587779693
Varsomers587779693
Maprs587779693
PheGenIrs587779693
hapmaprs587779693
1000 genomesrs587779693
hgdprs587779693
ensemblrs587779693
gopubmedrs587779693
geneviewrs587779693
scholarrs587779693
googlers587779693
pharmgkbrs587779693
gwascentralrs587779693
openSNPrs587779693
23andMers587779693
23andMe allrs587779693
SNP Nexus

SNPshotrs587779693
SNPdbers587779693
MSV3drs587779693
GWAS Ctlgrs587779693
Max Magnitude0
ClinVar
Risk rs587779693(A;A)
Alt rs587779693(A;A)
Reference rs587779693(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.189860464G>A
CLNSRC Ehlers-Danlos Syndrome Variant Database COL3A1
CLNACC RCV000087691.1,