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rs587779702

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779702(-;-)
Make rs587779702(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position188996126
GeneCOL3A1, MIR3606
is asnp
is mentioned by
dbSNPrs587779702
ebirs587779702
HLIrs587779702
Exacrs587779702
Varsomers587779702
Maprs587779702
PheGenIrs587779702
hapmaprs587779702
1000 genomesrs587779702
hgdprs587779702
ensemblrs587779702
gopubmedrs587779702
geneviewrs587779702
scholarrs587779702
googlers587779702
pharmgkbrs587779702
gwascentralrs587779702
openSNPrs587779702
23andMers587779702
23andMe allrs587779702
SNP Nexus

SNPshotrs587779702
SNPdbers587779702
MSV3drs587779702
GWAS Ctlgrs587779702
Max Magnitude0
ClinVar
Risk rs587779702(;)
Alt rs587779702(;)
Reference rs587779702(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.189860852delG
CLNSRC
CLNACC RCV000087703.1,