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rs587779608

From SNPedia

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Geno Mag Summary
(;) 0 common in clinvar
Make rs587779608(-;-)
Make rs587779608(-;T)
Make rs587779608(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position188997176
GeneCOL3A1
is asnp
is mentioned by
dbSNPrs587779608
ebirs587779608
HLIrs587779608
Exacrs587779608
Varsomers587779608
Maprs587779608
PheGenIrs587779608
hapmaprs587779608
1000 genomesrs587779608
hgdprs587779608
ensemblrs587779608
gopubmedrs587779608
geneviewrs587779608
scholarrs587779608
googlers587779608
pharmgkbrs587779608
gwascentralrs587779608
openSNPrs587779608
23andMers587779608
23andMe allrs587779608
SNP Nexus

SNPshotrs587779608
SNPdbers587779608
MSV3drs587779608
GWAS Ctlgrs587779608
Max Magnitude0
ClinVar
Risk rs587779608(T;T)
Alt rs587779608(T;T)
Reference rs587779608(;)
Significance Pathogenic
Disease Ehlers-Danlos syndrome
Variation info
Gene COL3A1
CLNDBN Ehlers-Danlos syndrome, type 4
Reversed 0
HGVS NC_000002.11:g.189861902dupT
CLNSRC Ehlers-Danlos Syndrome Variant Database COL3A1
CLNACC RCV000087563.1,