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rs587779433

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779433(C;C)
Make rs587779433(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position188998683
GeneCOL3A1
is asnp
is mentioned by
dbSNPrs587779433
ebirs587779433
HLIrs587779433
Exacrs587779433
Varsomers587779433
Maprs587779433
PheGenIrs587779433
hapmaprs587779433
1000 genomesrs587779433
hgdprs587779433
ensemblrs587779433
gopubmedrs587779433
geneviewrs587779433
scholarrs587779433
googlers587779433
pharmgkbrs587779433
gwascentralrs587779433
openSNPrs587779433
23andMers587779433
23andMe allrs587779433
SNP Nexus

SNPshotrs587779433
SNPdbers587779433
MSV3drs587779433
GWAS Ctlgrs587779433
Max Magnitude0
ClinVar
Risk rs587779433(C;C)
Alt rs587779433(C;C)
Reference rs587779433(G;G)
Significance Pathogenic
Disease Ehlers-Danlos syndrome not provided
Variation info
Gene COL3A1
CLNDBN Ehlers-Danlos syndrome, type 4 not provided
Reversed 0
HGVS NC_000002.11:g.189863409G>C
CLNSRC
CLNACC RCV000087357.1, RCV000181090.2,