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rs587780588

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587780588(A;A)
Make rs587780588(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position110183002
GeneCOL4A1
is asnp
is mentioned by
dbSNPrs587780588
ebirs587780588
HLIrs587780588
Exacrs587780588
Varsomers587780588
Maprs587780588
PheGenIrs587780588
hapmaprs587780588
1000 genomesrs587780588
hgdprs587780588
ensemblrs587780588
gopubmedrs587780588
geneviewrs587780588
scholarrs587780588
googlers587780588
pharmgkbrs587780588
gwascentralrs587780588
openSNPrs587780588
23andMers587780588
23andMe allrs587780588
SNP Nexus

SNPshotrs587780588
SNPdbers587780588
MSV3drs587780588
GWAS Ctlgrs587780588
Max Magnitude0
ClinVar
Risk rs587780588(A;A)
Alt rs587780588(A;A)
Reference rs587780588(G;G)
Significance Probable-Pathogenic
Disease Brain small vessel disease with hemorrhage
Variation info
Gene COL4A1
CLNDBN Brain small vessel disease with hemorrhage
Reversed 1
HGVS NC_000013.10:g.110835349C>T
CLNSRC
CLNACC RCV000122731.1,