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rs121912857

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912857(A;A)
Make rs121912857(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position110187181
GeneCOL4A1
is asnp
is mentioned by
dbSNPrs121912857
ebirs121912857
HLIrs121912857
Exacrs121912857
Varsomers121912857
Maprs121912857
PheGenIrs121912857
hapmaprs121912857
1000 genomesrs121912857
hgdprs121912857
ensemblrs121912857
gopubmedrs121912857
geneviewrs121912857
scholarrs121912857
googlers121912857
pharmgkbrs121912857
gwascentralrs121912857
openSNPrs121912857
23andMers121912857
23andMe allrs121912857
SNP Nexus

SNPshotrs121912857
SNPdbers121912857
MSV3drs121912857
GWAS Ctlgrs121912857
Max Magnitude0
OMIM120130
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121912857(A;A)
Alt rs121912857(A;A)
Reference rs121912857(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.110839528C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018957.30,