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rs863223452

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223452(A;A)
Make rs863223452(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position134815629
GeneCOL5A1
is asnp
is mentioned by
dbSNPrs863223452
ebirs863223452
HLIrs863223452
Exacrs863223452
Varsomers863223452
Maprs863223452
PheGenIrs863223452
hapmaprs863223452
1000 genomesrs863223452
hgdprs863223452
ensemblrs863223452
gopubmedrs863223452
geneviewrs863223452
scholarrs863223452
googlers863223452
pharmgkbrs863223452
gwascentralrs863223452
openSNPrs863223452
23andMers863223452
23andMe allrs863223452
SNP Nexus

SNPshotrs863223452
SNPdbers863223452
MSV3drs863223452
GWAS Ctlgrs863223452
Max Magnitude0
ClinVar
Risk rs863223452(A;A)
Alt rs863223452(A;A)
Reference rs863223452(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene COL5A1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.137707475G>A
CLNSRC
CLNACC RCV000197960.1,