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rs672601349

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs672601349(A;A)
Make rs672601349(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position110181363
GeneCOL4A1
is asnp
is mentioned by
dbSNPrs672601349
ebirs672601349
HLIrs672601349
Exacrs672601349
Varsomers672601349
Maprs672601349
PheGenIrs672601349
hapmaprs672601349
1000 genomesrs672601349
hgdprs672601349
ensemblrs672601349
gopubmedrs672601349
geneviewrs672601349
scholarrs672601349
googlers672601349
pharmgkbrs672601349
gwascentralrs672601349
openSNPrs672601349
23andMers672601349
23andMe allrs672601349
SNP Nexus

SNPshotrs672601349
SNPdbers672601349
MSV3drs672601349
GWAS Ctlgrs672601349
Max Magnitude0
ClinVar
Risk rs672601349(A;A)
Alt rs672601349(A;A)
Reference rs672601349(G;G)
Significance 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.110833710C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000149402.4,