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rs113994107

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs113994107(A;A)
Make rs113994107(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position110186513
GeneCOL4A1
is asnp
is mentioned by
dbSNPrs113994107
ebirs113994107
HLIrs113994107
Exacrs113994107
Varsomers113994107
Maprs113994107
PheGenIrs113994107
hapmaprs113994107
1000 genomesrs113994107
hgdprs113994107
ensemblrs113994107
gopubmedrs113994107
geneviewrs113994107
scholarrs113994107
googlers113994107
pharmgkbrs113994107
gwascentralrs113994107
openSNPrs113994107
23andMers113994107
23andMe allrs113994107
SNP Nexus

SNPshotrs113994107
SNPdbers113994107
MSV3drs113994107
GWAS Ctlgrs113994107
Max Magnitude0
OMIM120130
Desc
Variant0003
Relatedalso
ClinVar
Risk rs113994107(A;A)
Alt rs113994107(A;A)
Reference rs113994107(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.110838860C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000032213.1,