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rs587777379

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777379(C;T)
Make rs587777379(T;T)
ReferenceGRCh38 38.1/142
Chromosome13
Position110166277
GeneCOL4A1
is asnp
is mentioned by
dbSNPrs587777379
ebirs587777379
HLIrs587777379
Exacrs587777379
Varsomers587777379
Maprs587777379
PheGenIrs587777379
hapmaprs587777379
1000 genomesrs587777379
hgdprs587777379
ensemblrs587777379
gopubmedrs587777379
geneviewrs587777379
scholarrs587777379
googlers587777379
pharmgkbrs587777379
gwascentralrs587777379
openSNPrs587777379
23andMers587777379
23andMe allrs587777379
SNP Nexus

SNPshotrs587777379
SNPdbers587777379
MSV3drs587777379
GWAS Ctlgrs587777379
Max Magnitude0
ClinVar
Risk rs587777379(C,T;C,T)
Alt rs587777379(C,T;C,T)
Reference rs587777379(G;G)
Significance Pathogenic
Disease SCHIZENCEPHALY
Variation info
Gene COL4A1
CLNDBN SCHIZENCEPHALY
Reversed 1
HGVS NC_000013.10:g.110818624C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000119260.3,