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rs587779687

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779687(C;C)
Make rs587779687(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position188992886
GeneCOL3A1
is asnp
is mentioned by
dbSNPrs587779687
ebirs587779687
HLIrs587779687
Exacrs587779687
Varsomers587779687
Maprs587779687
PheGenIrs587779687
hapmaprs587779687
1000 genomesrs587779687
hgdprs587779687
ensemblrs587779687
gopubmedrs587779687
geneviewrs587779687
scholarrs587779687
googlers587779687
pharmgkbrs587779687
gwascentralrs587779687
openSNPrs587779687
23andMers587779687
23andMe allrs587779687
SNP Nexus

SNPshotrs587779687
SNPdbers587779687
MSV3drs587779687
GWAS Ctlgrs587779687
Max Magnitude0
ClinVar
Risk rs587779687(C;C)
Alt rs587779687(C;C)
Reference rs587779687(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.189857612G>C
CLNSRC
CLNACC RCV000087685.1, RCV000181075.2,