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rs113994105

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs113994105(A;A)
Make rs113994105(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position110187311
GeneCOL4A1
is asnp
is mentioned by
dbSNPrs113994105
ebirs113994105
HLIrs113994105
Exacrs113994105
Varsomers113994105
Maprs113994105
PheGenIrs113994105
hapmaprs113994105
1000 genomesrs113994105
hgdprs113994105
ensemblrs113994105
gopubmedrs113994105
geneviewrs113994105
scholarrs113994105
googlers113994105
pharmgkbrs113994105
gwascentralrs113994105
openSNPrs113994105
23andMers113994105
23andMe allrs113994105
SNP Nexus

SNPshotrs113994105
SNPdbers113994105
MSV3drs113994105
GWAS Ctlgrs113994105
Max Magnitude0
OMIM120130
Desc
Variant0008
Relatedalso
ClinVar
Risk rs113994105(A;A)
Alt rs113994105(A;A)
Reference rs113994105(G;G)
Significance Pathogenic
Disease Angiopathy
Variation info
Gene COL4A1
CLNDBN Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps
Reversed 1
HGVS NC_000013.10:g.110839658C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018962.28,