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rs672601348

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs672601348(C;G)
Make rs672601348(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position110152381
GeneCOL4A1
is asnp
is mentioned by
dbSNPrs672601348
ebirs672601348
HLIrs672601348
Exacrs672601348
Varsomers672601348
Maprs672601348
PheGenIrs672601348
hapmaprs672601348
1000 genomesrs672601348
hgdprs672601348
ensemblrs672601348
gopubmedrs672601348
geneviewrs672601348
scholarrs672601348
googlers672601348
pharmgkbrs672601348
gwascentralrs672601348
openSNPrs672601348
23andMers672601348
23andMe allrs672601348
SNP Nexus

SNPshotrs672601348
SNPdbers672601348
MSV3drs672601348
GWAS Ctlgrs672601348
Max Magnitude0
ClinVar
Risk rs672601348(G,T;G,T)
Alt rs672601348(G,T;G,T)
Reference rs672601348(C;C)
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.110804728G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000149401.5,