Have questions? Visit https://www.reddit.com/r/SNPedia

rs387906602

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906602(A;A)
Make rs387906602(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position110492070
GeneCOL4A2
is asnp
is mentioned by
dbSNPrs387906602
ebirs387906602
HLIrs387906602
Exacrs387906602
Varsomers387906602
Maprs387906602
PheGenIrs387906602
hapmaprs387906602
1000 genomesrs387906602
hgdprs387906602
ensemblrs387906602
gopubmedrs387906602
geneviewrs387906602
scholarrs387906602
googlers387906602
pharmgkbrs387906602
gwascentralrs387906602
openSNPrs387906602
23andMers387906602
23andMe allrs387906602
SNP Nexus

SNPshotrs387906602
SNPdbers387906602
MSV3drs387906602
GWAS Ctlgrs387906602
Max Magnitude0
ClinVar
Risk rs387906602(A;A)
Alt rs387906602(A;A)
Reference rs387906602(G;G)
Significance Pathogenic
Disease Porencephaly 2
Variation info
Gene COL4A2
CLNDBN Porencephaly 2
Reversed 0
HGVS NC_000013.10:g.111144417G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022467.23,