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rs587779701

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779701(G;G)
Make rs587779701(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position188995036
GeneCOL3A1, MIR3606
is asnp
is mentioned by
dbSNPrs587779701
ebirs587779701
HLIrs587779701
Exacrs587779701
Varsomers587779701
Maprs587779701
PheGenIrs587779701
hapmaprs587779701
1000 genomesrs587779701
hgdprs587779701
ensemblrs587779701
gopubmedrs587779701
geneviewrs587779701
scholarrs587779701
googlers587779701
pharmgkbrs587779701
gwascentralrs587779701
openSNPrs587779701
23andMers587779701
23andMe allrs587779701
SNP Nexus

SNPshotrs587779701
SNPdbers587779701
MSV3drs587779701
GWAS Ctlgrs587779701
Max Magnitude0
ClinVar
Risk rs587779701(G;G)
Alt rs587779701(G;G)
Reference rs587779701(T;T)
Significance Pathogenic
Disease Ehlers-Danlos syndrome
Variation info
Gene COL3A1 MIR3606
CLNDBN Ehlers-Danlos syndrome, type 4
Reversed 0
HGVS NC_000002.11:g.189859762T>G
CLNSRC
CLNACC RCV000087702.1,