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

rs587779641

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779641(A;A)
Make rs587779641(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position188988600
GeneCOL3A1
is asnp
is mentioned by
dbSNPrs587779641
ebirs587779641
HLIrs587779641
Exacrs587779641
Varsomers587779641
Maprs587779641
PheGenIrs587779641
hapmaprs587779641
1000 genomesrs587779641
hgdprs587779641
ensemblrs587779641
gopubmedrs587779641
geneviewrs587779641
scholarrs587779641
googlers587779641
pharmgkbrs587779641
gwascentralrs587779641
openSNPrs587779641
23andMers587779641
23andMe allrs587779641
SNP Nexus

SNPshotrs587779641
SNPdbers587779641
MSV3drs587779641
GWAS Ctlgrs587779641
Max Magnitude0
ClinVar
Risk rs587779641(A;A)
Alt rs587779641(A;A)
Reference rs587779641(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.189853326G>A
CLNSRC
CLNACC RCV000087611.1,