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rs267606743

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606743(A;A)
Make rs267606743(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position110192222
GeneCOL4A1
is asnp
is mentioned by
dbSNPrs267606743
ebirs267606743
HLIrs267606743
Exacrs267606743
Varsomers267606743
Maprs267606743
PheGenIrs267606743
hapmaprs267606743
1000 genomesrs267606743
hgdprs267606743
ensemblrs267606743
gopubmedrs267606743
geneviewrs267606743
scholarrs267606743
googlers267606743
pharmgkbrs267606743
gwascentralrs267606743
openSNPrs267606743
23andMers267606743
23andMe allrs267606743
SNP Nexus

SNPshotrs267606743
SNPdbers267606743
MSV3drs267606743
GWAS Ctlgrs267606743
Max Magnitude0
ClinVar
Risk rs267606743(A;A)
Alt rs267606743(A;A)
Reference rs267606743(G;G)
Significance Pathogenic
Disease Angiopathy Retinal arteries
Variation info
Gene COL4A1
CLNDBN Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps Retinal arteries, tortuosity of
Reversed 1
HGVS NC_000013.10:g.110844569C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018967.29, RCV000170340.4,