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rs113994108

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs113994108(A;A)
Make rs113994108(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position110181326
GeneCOL4A1
is asnp
is mentioned by
dbSNPrs113994108
ebirs113994108
HLIrs113994108
Exacrs113994108
Varsomers113994108
Maprs113994108
PheGenIrs113994108
hapmaprs113994108
1000 genomesrs113994108
hgdprs113994108
ensemblrs113994108
gopubmedrs113994108
geneviewrs113994108
scholarrs113994108
googlers113994108
pharmgkbrs113994108
gwascentralrs113994108
openSNPrs113994108
23andMers113994108
23andMe allrs113994108
SNP Nexus

SNPshotrs113994108
SNPdbers113994108
MSV3drs113994108
GWAS Ctlgrs113994108
Max Magnitude0
OMIM120130
Desc
Variant0010
Relatedalso
ClinVar
Risk rs113994108(A;A)
Alt rs113994108(A;A)
Reference rs113994108(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.110833673C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032214.4,