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rs672601347

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs672601347(C;C)
Make rs672601347(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position110179298
GeneCOL4A1
is asnp
is mentioned by
dbSNPrs672601347
dbSNP (old)rs672601347
ClinGenrs672601347
ebirs672601347
HLIrs672601347
Exacrs672601347
Gnomadrs672601347
Varsomers672601347
Maprs672601347
PheGenIrs672601347
Biobankrs672601347
1000 genomesrs672601347
hgdprs672601347
ensemblrs672601347
gopubmedrs672601347
geneviewrs672601347
scholarrs672601347
googlers672601347
pharmgkbrs672601347
gwascentralrs672601347
openSNPrs672601347
23andMers672601347
23andMe allrs672601347
SNP Nexus

SNPshotrs672601347
SNPdbers672601347
MSV3drs672601347
GWAS Ctlgrs672601347
Max Magnitude0
ClinVar
Risk rs672601347(A;A) rs672601347(C;C)
Alt rs672601347(A;A) rs672601347(C;C)
Reference Rs672601347(G;G)
Significance Pathogenic
Disease Brain small vessel disease with hemorrhage not provided
Variation info
Gene COL4A1
CLNDBN Brain small vessel disease with hemorrhage not provided
Reversed 1
HGVS NC_000013.10:g.110831645C>G; NC_000013.10:g.110831645C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000149400.6, RCV000437521.1,