Have questions? Visit https://www.reddit.com/r/SNPedia

rs587779634

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779634(A;A)
Make rs587779634(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position188997364
GeneCOL3A1
is asnp
is mentioned by
dbSNPrs587779634
ebirs587779634
HLIrs587779634
Exacrs587779634
Varsomers587779634
Maprs587779634
PheGenIrs587779634
hapmaprs587779634
1000 genomesrs587779634
hgdprs587779634
ensemblrs587779634
gopubmedrs587779634
geneviewrs587779634
scholarrs587779634
googlers587779634
pharmgkbrs587779634
gwascentralrs587779634
openSNPrs587779634
23andMers587779634
23andMe allrs587779634
SNP Nexus

SNPshotrs587779634
SNPdbers587779634
MSV3drs587779634
GWAS Ctlgrs587779634
Max Magnitude0
ClinVar
Risk rs587779634(A;A)
Alt rs587779634(A;A)
Reference rs587779634(G;G)
Significance Pathogenic
Disease Ehlers-Danlos syndrome
Variation info
Gene COL3A1
CLNDBN Ehlers-Danlos syndrome, type 4
Reversed 0
HGVS NC_000002.11:g.189862090G>A
CLNSRC Ehlers-Danlos Syndrome Variant Database COL3A1
CLNACC RCV000087604.1,