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rs863223466

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223466(A;A)
Make rs863223466(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position134731663
GeneCOL5A1
is asnp
is mentioned by
dbSNPrs863223466
ebirs863223466
HLIrs863223466
Exacrs863223466
Varsomers863223466
Maprs863223466
PheGenIrs863223466
hapmaprs863223466
1000 genomesrs863223466
hgdprs863223466
ensemblrs863223466
gopubmedrs863223466
geneviewrs863223466
scholarrs863223466
googlers863223466
pharmgkbrs863223466
gwascentralrs863223466
openSNPrs863223466
23andMers863223466
23andMe allrs863223466
SNP Nexus

SNPshotrs863223466
SNPdbers863223466
MSV3drs863223466
GWAS Ctlgrs863223466
Max Magnitude0
ClinVar
Risk rs863223466(A;A)
Alt rs863223466(A;A)
Reference rs863223466(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL5A1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.137623509G>A
CLNSRC
CLNACC RCV000200548.1,