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rs606231465

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs606231465(A;A)
Make rs606231465(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position110179422
GeneCOL4A1
is asnp
is mentioned by
dbSNPrs606231465
ebirs606231465
HLIrs606231465
Exacrs606231465
Varsomers606231465
Maprs606231465
PheGenIrs606231465
hapmaprs606231465
1000 genomesrs606231465
hgdprs606231465
ensemblrs606231465
gopubmedrs606231465
geneviewrs606231465
scholarrs606231465
googlers606231465
pharmgkbrs606231465
gwascentralrs606231465
openSNPrs606231465
23andMers606231465
23andMe allrs606231465
SNP Nexus

SNPshotrs606231465
SNPdbers606231465
MSV3drs606231465
GWAS Ctlgrs606231465
Max Magnitude0
ClinVar
Risk rs606231465(A;A)
Alt rs606231465(A;A)
Reference rs606231465(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.110831769C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000148944.5,