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rs587779607

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779607(C;T)
Make rs587779607(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position188992208
GeneCOL3A1
is asnp
is mentioned by
dbSNPrs587779607
ebirs587779607
HLIrs587779607
Exacrs587779607
Varsomers587779607
Maprs587779607
PheGenIrs587779607
hapmaprs587779607
1000 genomesrs587779607
hgdprs587779607
ensemblrs587779607
gopubmedrs587779607
geneviewrs587779607
scholarrs587779607
googlers587779607
pharmgkbrs587779607
gwascentralrs587779607
openSNPrs587779607
23andMers587779607
23andMe allrs587779607
SNP Nexus

SNPshotrs587779607
SNPdbers587779607
MSV3drs587779607
GWAS Ctlgrs587779607
Max Magnitude0
ClinVar
Risk rs587779607(T;T)
Alt rs587779607(T;T)
Reference rs587779607(C;C)
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.189856934C>T
CLNSRC
CLNACC RCV000087562.1, RCV000181122.1,