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

rs587779505

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779505(A;A)
Make rs587779505(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position189004028
GeneCOL3A1
is asnp
is mentioned by
dbSNPrs587779505
ebirs587779505
HLIrs587779505
Exacrs587779505
Varsomers587779505
Maprs587779505
PheGenIrs587779505
hapmaprs587779505
1000 genomesrs587779505
hgdprs587779505
ensemblrs587779505
gopubmedrs587779505
geneviewrs587779505
scholarrs587779505
googlers587779505
pharmgkbrs587779505
gwascentralrs587779505
openSNPrs587779505
23andMers587779505
23andMe allrs587779505
SNP Nexus

SNPshotrs587779505
SNPdbers587779505
MSV3drs587779505
GWAS Ctlgrs587779505
Max Magnitude0
ClinVar
Risk rs587779505(A;A)
Alt rs587779505(A;A)
Reference rs587779505(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.189868754G>A
CLNSRC Ehlers-Danlos Syndrome Variant Database COL3A1
CLNACC RCV000087440.1,