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rs587779496

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779496(G;G)
Make rs587779496(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position188994538
GeneCOL3A1, MIR3606
is asnp
is mentioned by
dbSNPrs587779496
ebirs587779496
HLIrs587779496
Exacrs587779496
Varsomers587779496
Maprs587779496
PheGenIrs587779496
hapmaprs587779496
1000 genomesrs587779496
hgdprs587779496
ensemblrs587779496
gopubmedrs587779496
geneviewrs587779496
scholarrs587779496
googlers587779496
pharmgkbrs587779496
gwascentralrs587779496
openSNPrs587779496
23andMers587779496
23andMe allrs587779496
SNP Nexus

SNPshotrs587779496
SNPdbers587779496
MSV3drs587779496
GWAS Ctlgrs587779496
Max Magnitude0
ClinVar
Risk rs587779496(G;G)
Alt rs587779496(G;G)
Reference rs587779496(T;T)
Significance Pathogenic
Disease Ehlers-Danlos syndrome
Variation info
Gene COL3A1 MIR3606
CLNDBN Ehlers-Danlos syndrome, type 4
Reversed 0
HGVS NC_000002.11:g.189859264T>G
CLNSRC
CLNACC RCV000087430.1,