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rs672601346

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs672601346(A;A)
Make rs672601346(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position110179352
GeneCOL4A1
is asnp
is mentioned by
dbSNPrs672601346
ebirs672601346
HLIrs672601346
Exacrs672601346
Varsomers672601346
Maprs672601346
PheGenIrs672601346
hapmaprs672601346
1000 genomesrs672601346
hgdprs672601346
ensemblrs672601346
gopubmedrs672601346
geneviewrs672601346
scholarrs672601346
googlers672601346
pharmgkbrs672601346
gwascentralrs672601346
openSNPrs672601346
23andMers672601346
23andMe allrs672601346
SNP Nexus

SNPshotrs672601346
SNPdbers672601346
MSV3drs672601346
GWAS Ctlgrs672601346
Max Magnitude0
ClinVar
Risk rs672601346(A;A)
Alt rs672601346(A;A)
Reference rs672601346(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.110831699C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000149399.4,