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rs863223458

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223458(A;A)
Make rs863223458(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position134820143
GeneCOL5A1, LOC101448202
is asnp
is mentioned by
dbSNPrs863223458
ebirs863223458
HLIrs863223458
Exacrs863223458
Varsomers863223458
Maprs863223458
PheGenIrs863223458
hapmaprs863223458
1000 genomesrs863223458
hgdprs863223458
ensemblrs863223458
gopubmedrs863223458
geneviewrs863223458
scholarrs863223458
googlers863223458
pharmgkbrs863223458
gwascentralrs863223458
openSNPrs863223458
23andMers863223458
23andMe allrs863223458
SNP Nexus

SNPshotrs863223458
SNPdbers863223458
MSV3drs863223458
GWAS Ctlgrs863223458
Max Magnitude0
ClinVar
Risk rs863223458(A;A)
Alt rs863223458(A;A)
Reference rs863223458(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene COL5A1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.137711989G>A
CLNSRC
CLNACC RCV000200200.1,